Incidental Mutation 'R3808:Fgfr2'
ID 473946
Institutional Source Beutler Lab
Gene Symbol Fgfr2
Ensembl Gene ENSMUSG00000030849
Gene Name fibroblast growth factor receptor 2
Synonyms KGFRTr, svs, Bek, Fgfr-2, Fgfr2b, Fgfr-7, Fgfr7
MMRRC Submission 040765-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R3808 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 129764181-129868538 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 129801578 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 218 (M218V)
Ref Sequence ENSEMBL: ENSMUSP00000112585 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000117073] [ENSMUST00000117089] [ENSMUST00000117357] [ENSMUST00000117691] [ENSMUST00000117754] [ENSMUST00000117858] [ENSMUST00000122448] [ENSMUST00000118296] [ENSMUST00000120141] [ENSMUST00000120187] [ENSMUST00000121064] [ENSMUST00000121080] [ENSMUST00000119260] [ENSMUST00000117872] [ENSMUST00000122054] [ENSMUST00000124096] [ENSMUST00000120715] [ENSMUST00000153166]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000117073
SMART Domains Protein: ENSMUSP00000112672
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 55 123 4.66e-13 SMART
IGc2 154 234 7.41e-7 SMART
transmembrane domain 260 282 N/A INTRINSIC
low complexity region 314 323 N/A INTRINSIC
TyrKc 364 640 4.38e-152 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000117089
AA Change: M333V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000112992
Gene: ENSMUSG00000030849
AA Change: M333V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 31 40 N/A INTRINSIC
IGc2 53 114 6.59e-13 SMART
low complexity region 129 146 N/A INTRINSIC
IGc2 170 238 4.66e-13 SMART
IGc2 269 347 1.9e-4 SMART
transmembrane domain 376 398 N/A INTRINSIC
low complexity region 430 439 N/A INTRINSIC
TyrKc 480 756 4.38e-152 SMART
low complexity region 784 798 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117357
AA Change: M218V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000112580
Gene: ENSMUSG00000030849
AA Change: M218V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 55 123 4.66e-13 SMART
IGc2 154 232 1.9e-4 SMART
transmembrane domain 261 283 N/A INTRINSIC
low complexity region 315 324 N/A INTRINSIC
TyrKc 365 641 4.38e-152 SMART
low complexity region 669 683 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117691
AA Change: M333V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000113180
Gene: ENSMUSG00000030849
AA Change: M333V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 31 40 N/A INTRINSIC
IGc2 53 114 6.59e-13 SMART
low complexity region 129 146 N/A INTRINSIC
IGc2 170 238 4.66e-13 SMART
IGc2 269 347 1.9e-4 SMART
transmembrane domain 376 398 N/A INTRINSIC
low complexity region 432 441 N/A INTRINSIC
TyrKc 482 758 4.38e-152 SMART
low complexity region 786 800 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117754
SMART Domains Protein: ENSMUSP00000113187
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 56 136 7.41e-7 SMART
transmembrane domain 162 184 N/A INTRINSIC
low complexity region 218 227 N/A INTRINSIC
TyrKc 268 544 4.38e-152 SMART
low complexity region 572 586 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117858
AA Change: M333V

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000112623
Gene: ENSMUSG00000030849
AA Change: M333V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 31 40 N/A INTRINSIC
IGc2 53 114 6.59e-13 SMART
low complexity region 129 146 N/A INTRINSIC
IGc2 170 238 4.66e-13 SMART
IGc2 269 347 1.9e-4 SMART
transmembrane domain 376 398 N/A INTRINSIC
low complexity region 432 441 N/A INTRINSIC
TyrKc 482 758 4.38e-152 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000122448
AA Change: M218V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000113993
Gene: ENSMUSG00000030849
AA Change: M218V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 55 123 4.66e-13 SMART
IGc2 154 232 1.9e-4 SMART
transmembrane domain 261 283 N/A INTRINSIC
low complexity region 315 324 N/A INTRINSIC
TyrKc 365 641 4.38e-152 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000118296
AA Change: M244V

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000112471
Gene: ENSMUSG00000030849
AA Change: M244V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 36 57 N/A INTRINSIC
IGc2 81 149 4.66e-13 SMART
IGc2 180 258 1.9e-4 SMART
transmembrane domain 287 309 N/A INTRINSIC
low complexity region 343 352 N/A INTRINSIC
TyrKc 393 669 4.38e-152 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000120141
AA Change: M244V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000113415
Gene: ENSMUSG00000030849
AA Change: M244V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 36 57 N/A INTRINSIC
IGc2 81 149 4.66e-13 SMART
IGc2 180 258 1.9e-4 SMART
transmembrane domain 287 309 N/A INTRINSIC
low complexity region 341 350 N/A INTRINSIC
TyrKc 391 667 4.38e-152 SMART
low complexity region 695 709 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000120187
AA Change: M237V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000113248
Gene: ENSMUSG00000030849
AA Change: M237V

DomainStartEndE-ValueType
transmembrane domain 15 37 N/A INTRINSIC
IGc2 74 142 4.66e-13 SMART
IGc2 173 251 1.9e-4 SMART
transmembrane domain 280 302 N/A INTRINSIC
low complexity region 336 345 N/A INTRINSIC
TyrKc 386 662 4.38e-152 SMART
low complexity region 690 704 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000121064
AA Change: M120V

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000113452
Gene: ENSMUSG00000030849
AA Change: M120V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 56 134 1.9e-4 SMART
transmembrane domain 163 185 N/A INTRINSIC
low complexity region 219 228 N/A INTRINSIC
TyrKc 269 545 4.38e-152 SMART
low complexity region 573 587 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000121080
AA Change: M218V

PolyPhen 2 Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000112585
Gene: ENSMUSG00000030849
AA Change: M218V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 55 123 4.66e-13 SMART
IGc2 154 232 1.9e-4 SMART
transmembrane domain 261 283 N/A INTRINSIC
low complexity region 317 326 N/A INTRINSIC
TyrKc 367 643 4.38e-152 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000127091
SMART Domains Protein: ENSMUSP00000122856
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
Pfam:I-set 3 56 1.8e-7 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000119260
SMART Domains Protein: ENSMUSP00000113010
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 31 40 N/A INTRINSIC
IGc2 53 114 6.59e-13 SMART
low complexity region 129 146 N/A INTRINSIC
IGc2 170 238 4.66e-13 SMART
IGc2 269 349 7.41e-7 SMART
transmembrane domain 375 397 N/A INTRINSIC
low complexity region 429 438 N/A INTRINSIC
TyrKc 479 755 4.38e-152 SMART
low complexity region 783 797 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117872
SMART Domains Protein: ENSMUSP00000113994
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
transmembrane domain 15 37 N/A INTRINSIC
IGc2 74 142 4.66e-13 SMART
IGc2 173 253 7.41e-7 SMART
transmembrane domain 279 301 N/A INTRINSIC
low complexity region 333 342 N/A INTRINSIC
TyrKc 383 659 4.38e-152 SMART
low complexity region 687 701 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000122054
SMART Domains Protein: ENSMUSP00000112430
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
transmembrane domain 15 37 N/A INTRINSIC
low complexity region 50 59 N/A INTRINSIC
IGc2 72 133 6.59e-13 SMART
low complexity region 148 165 N/A INTRINSIC
IGc2 189 257 4.66e-13 SMART
IGc2 288 368 7.41e-7 SMART
transmembrane domain 394 416 N/A INTRINSIC
low complexity region 450 459 N/A INTRINSIC
TyrKc 500 776 4.38e-152 SMART
low complexity region 804 818 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000124096
SMART Domains Protein: ENSMUSP00000130971
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
Pfam:Pkinase 1 118 4.8e-19 PFAM
Pfam:Pkinase_Tyr 1 118 1.7e-50 PFAM
low complexity region 146 160 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000120715
SMART Domains Protein: ENSMUSP00000113474
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 31 40 N/A INTRINSIC
IGc2 53 114 6.59e-13 SMART
low complexity region 129 146 N/A INTRINSIC
IGc2 170 238 4.66e-13 SMART
transmembrane domain 263 285 N/A INTRINSIC
low complexity region 319 328 N/A INTRINSIC
TyrKc 369 645 4.38e-152 SMART
low complexity region 673 687 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148675
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133806
Predicted Effect probably benign
Transcript: ENSMUST00000153166
SMART Domains Protein: ENSMUSP00000120100
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
transmembrane domain 21 40 N/A INTRINSIC
low complexity region 50 59 N/A INTRINSIC
IGc2 72 133 6.59e-13 SMART
low complexity region 148 165 N/A INTRINSIC
IGc2 189 257 4.66e-13 SMART
SCOP:d1ev2e1 269 311 1e-5 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 95.8%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, depending on the isoform. Mutations in this gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis. Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]
PHENOTYPE: Mice homozygous for null mutations die as embryos. Isoform IIIb deficient mutants die at birth with defects in multiple organs and tissues. Isoform IIIc deficient mutants have defects in osteoblast and chondrocyte lineages, producing dwarfism. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik G T 12: 71,211,320 (GRCm39) E685* probably null Het
2700049A03Rik A T 12: 71,211,321 (GRCm39) E685V possibly damaging Het
Aldh3a2 G T 11: 61,149,623 (GRCm39) L248M probably damaging Het
Als2 A G 1: 59,209,609 (GRCm39) S1458P probably benign Het
Aoc1l3 C T 6: 48,964,928 (GRCm39) P312L possibly damaging Het
Arhgap5 A G 12: 52,613,970 (GRCm39) E192G possibly damaging Het
Atg2a A G 19: 6,302,846 (GRCm39) K1019R possibly damaging Het
Atp2b1 A G 10: 98,839,010 (GRCm39) K613E possibly damaging Het
Carm1 T C 9: 21,498,258 (GRCm39) C421R probably damaging Het
Cdh17 A T 4: 11,795,671 (GRCm39) Y417F probably damaging Het
Cers1 A G 8: 70,782,660 (GRCm39) D10G possibly damaging Het
Clptm1l A C 13: 73,760,573 (GRCm39) M319L probably benign Het
Cntnap3 A G 13: 64,929,618 (GRCm39) V527A probably damaging Het
Creb3l2 A G 6: 37,332,625 (GRCm39) S290P probably damaging Het
Dock4 T G 12: 40,722,809 (GRCm39) V305G probably damaging Het
Dtl A C 1: 191,280,466 (GRCm39) L356R probably damaging Het
Eftud2 A T 11: 102,732,289 (GRCm39) probably null Het
Eif2b4 A G 5: 31,348,512 (GRCm39) S88P possibly damaging Het
Fat4 T G 3: 39,036,587 (GRCm39) V3413G possibly damaging Het
Grin2b A G 6: 135,900,269 (GRCm39) L204P probably damaging Het
Kcnj12 A G 11: 60,961,103 (GRCm39) N467S probably benign Het
Klhdc3 T A 17: 46,988,858 (GRCm39) N111Y possibly damaging Het
Lin9 A G 1: 180,486,676 (GRCm39) I81V probably null Het
Lrp2 T C 2: 69,331,892 (GRCm39) D1621G probably damaging Het
Lrp4 T A 2: 91,307,047 (GRCm39) D389E probably damaging Het
Med15 C T 16: 17,473,598 (GRCm39) probably benign Het
Nbea T C 3: 55,625,269 (GRCm39) N2274S probably benign Het
Nr3c2 G A 8: 77,635,343 (GRCm39) G148D probably damaging Het
Or10s1 A T 9: 39,985,605 (GRCm39) M5L probably benign Het
Or14j6 T C 17: 38,214,464 (GRCm39) V9A probably benign Het
Or4c112 G T 2: 88,853,770 (GRCm39) H192Q probably benign Het
Paxip1 A G 5: 27,977,027 (GRCm39) probably benign Het
Pfas T C 11: 68,880,779 (GRCm39) probably benign Het
Plin3 C A 17: 56,593,275 (GRCm39) A96S probably damaging Het
Pnck T A X: 72,700,550 (GRCm39) I288F probably damaging Het
Ppp4c C T 7: 126,386,499 (GRCm39) G166D probably damaging Het
Prss43 A T 9: 110,656,840 (GRCm39) R115S probably damaging Het
Rassf2 T C 2: 131,840,180 (GRCm39) probably null Het
Rdh16f1 T A 10: 127,624,568 (GRCm39) D135E probably benign Het
Rdh16f1 G A 10: 127,624,569 (GRCm39) V136M probably damaging Het
Rgs12 A G 5: 35,189,698 (GRCm39) E702G probably damaging Het
Rnf213 A G 11: 119,370,384 (GRCm39) K4728E probably damaging Het
Ros1 T G 10: 51,996,944 (GRCm39) T1243P probably benign Het
Sall1 G A 8: 89,758,101 (GRCm39) Q668* probably null Het
Sbf2 C A 7: 110,088,487 (GRCm39) *45L probably null Het
Serpina3j A T 12: 104,286,086 (GRCm39) I414F probably benign Het
Sh2d3c T C 2: 32,636,108 (GRCm39) Y159H probably damaging Het
Slamf1 A G 1: 171,625,745 (GRCm39) D307G probably null Het
Slc22a13 T C 9: 119,025,143 (GRCm39) T178A probably benign Het
Smchd1 A T 17: 71,736,536 (GRCm39) L588H probably damaging Het
Trim12a G A 7: 103,956,201 (GRCm39) A113V probably benign Het
Vil1 T C 1: 74,466,772 (GRCm39) V654A probably benign Het
Vmn1r202 T C 13: 22,686,070 (GRCm39) T116A possibly damaging Het
Zfp267 T G 3: 36,219,792 (GRCm39) probably null Het
Zfp607a G A 7: 27,578,826 (GRCm39) R632H probably benign Het
Other mutations in Fgfr2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00514:Fgfr2 APN 7 129,769,441 (GRCm39) missense probably benign 0.45
IGL00594:Fgfr2 APN 7 129,830,453 (GRCm39) missense probably damaging 1.00
IGL00963:Fgfr2 APN 7 129,830,491 (GRCm39) missense probably damaging 0.99
IGL01968:Fgfr2 APN 7 129,786,978 (GRCm39) missense probably damaging 1.00
IGL02003:Fgfr2 APN 7 129,820,802 (GRCm39) missense probably damaging 1.00
IGL02063:Fgfr2 APN 7 129,769,485 (GRCm39) missense probably damaging 1.00
IGL02239:Fgfr2 APN 7 129,779,416 (GRCm39) missense probably damaging 1.00
IGL02349:Fgfr2 APN 7 129,844,336 (GRCm39) missense probably damaging 1.00
IGL02630:Fgfr2 APN 7 129,830,525 (GRCm39) splice site probably null
IGL02639:Fgfr2 APN 7 129,830,532 (GRCm39) splice site probably benign
IGL03058:Fgfr2 APN 7 129,784,422 (GRCm39) missense probably damaging 1.00
IGL03263:Fgfr2 APN 7 129,782,149 (GRCm39) missense probably benign 0.12
IGL03377:Fgfr2 APN 7 129,800,247 (GRCm39) missense probably damaging 0.98
R0048:Fgfr2 UTSW 7 129,782,218 (GRCm39) splice site probably benign
R0048:Fgfr2 UTSW 7 129,782,218 (GRCm39) splice site probably benign
R0078:Fgfr2 UTSW 7 129,802,805 (GRCm39) missense possibly damaging 0.95
R0085:Fgfr2 UTSW 7 129,797,993 (GRCm39) missense probably damaging 0.99
R0278:Fgfr2 UTSW 7 129,863,592 (GRCm39) splice site probably null
R0335:Fgfr2 UTSW 7 129,797,979 (GRCm39) missense probably benign 0.00
R0557:Fgfr2 UTSW 7 129,820,811 (GRCm39) missense probably damaging 1.00
R0631:Fgfr2 UTSW 7 129,828,969 (GRCm39) intron probably benign
R0637:Fgfr2 UTSW 7 129,773,354 (GRCm39) missense possibly damaging 0.89
R0841:Fgfr2 UTSW 7 130,373,737 (GRCm39) unclassified probably benign
R0841:Fgfr2 UTSW 7 129,863,635 (GRCm39) missense probably benign 0.03
R1646:Fgfr2 UTSW 7 129,844,374 (GRCm39) missense probably damaging 1.00
R1670:Fgfr2 UTSW 7 129,782,187 (GRCm39) missense probably damaging 1.00
R1678:Fgfr2 UTSW 7 129,830,350 (GRCm39) splice site probably null
R1950:Fgfr2 UTSW 7 129,800,211 (GRCm39) missense probably damaging 0.96
R2393:Fgfr2 UTSW 7 129,828,968 (GRCm39) splice site probably null
R3706:Fgfr2 UTSW 7 129,800,161 (GRCm39) missense probably benign 0.31
R3717:Fgfr2 UTSW 7 129,784,487 (GRCm39) missense probably damaging 1.00
R3945:Fgfr2 UTSW 7 129,779,485 (GRCm39) missense possibly damaging 0.71
R4438:Fgfr2 UTSW 7 129,774,660 (GRCm39) nonsense probably null
R4718:Fgfr2 UTSW 7 129,863,518 (GRCm39) missense probably damaging 1.00
R4779:Fgfr2 UTSW 7 129,786,923 (GRCm39) intron probably benign
R4925:Fgfr2 UTSW 7 129,787,002 (GRCm39) missense probably damaging 1.00
R4932:Fgfr2 UTSW 7 129,843,007 (GRCm39) missense probably damaging 1.00
R4941:Fgfr2 UTSW 7 129,800,175 (GRCm39) missense probably benign 0.21
R4980:Fgfr2 UTSW 7 129,802,810 (GRCm39) missense probably damaging 1.00
R5304:Fgfr2 UTSW 7 129,769,504 (GRCm39) missense probably damaging 1.00
R5313:Fgfr2 UTSW 7 129,842,970 (GRCm39) missense probably benign 0.01
R5375:Fgfr2 UTSW 7 129,842,945 (GRCm39) missense possibly damaging 0.65
R5652:Fgfr2 UTSW 7 129,863,593 (GRCm39) missense probably damaging 1.00
R6120:Fgfr2 UTSW 7 129,830,420 (GRCm39) missense probably benign 0.24
R6347:Fgfr2 UTSW 7 129,863,487 (GRCm39) missense probably damaging 1.00
R6375:Fgfr2 UTSW 7 129,769,475 (GRCm39) missense probably damaging 1.00
R6475:Fgfr2 UTSW 7 129,802,850 (GRCm39) missense probably benign 0.03
R6481:Fgfr2 UTSW 7 129,787,008 (GRCm39) missense possibly damaging 0.85
R6494:Fgfr2 UTSW 7 129,800,280 (GRCm39) missense probably damaging 1.00
R6542:Fgfr2 UTSW 7 129,802,853 (GRCm39) missense probably benign 0.02
R7246:Fgfr2 UTSW 7 129,844,136 (GRCm39)
R7937:Fgfr2 UTSW 7 129,820,823 (GRCm39) missense probably damaging 1.00
R7976:Fgfr2 UTSW 7 129,787,074 (GRCm39) missense probably damaging 0.99
R8007:Fgfr2 UTSW 7 129,765,719 (GRCm39) nonsense probably null
R8189:Fgfr2 UTSW 7 129,774,629 (GRCm39) missense probably damaging 1.00
R8430:Fgfr2 UTSW 7 129,765,708 (GRCm39) missense probably damaging 1.00
R8486:Fgfr2 UTSW 7 129,765,745 (GRCm39) missense possibly damaging 0.93
R8489:Fgfr2 UTSW 7 129,769,534 (GRCm39) missense probably benign 0.01
R8776:Fgfr2 UTSW 7 129,798,002 (GRCm39) missense possibly damaging 0.64
R8776-TAIL:Fgfr2 UTSW 7 129,798,002 (GRCm39) missense possibly damaging 0.64
R9338:Fgfr2 UTSW 7 129,863,561 (GRCm39) nonsense probably null
R9340:Fgfr2 UTSW 7 129,782,136 (GRCm39) missense probably damaging 1.00
R9497:Fgfr2 UTSW 7 129,765,763 (GRCm39) missense probably damaging 1.00
RF016:Fgfr2 UTSW 7 129,779,410 (GRCm39) missense probably benign 0.03
X0024:Fgfr2 UTSW 7 129,787,059 (GRCm39) missense probably damaging 0.99
Z1088:Fgfr2 UTSW 7 129,771,529 (GRCm39) missense probably damaging 1.00
Z1177:Fgfr2 UTSW 7 129,800,187 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2017-04-14