Incidental Mutation 'R5970:Trav10d'
ID 470818
Institutional Source Beutler Lab
Gene Symbol Trav10d
Ensembl Gene ENSMUSG00000094792
Gene Name T cell receptor alpha variable 10D
MMRRC Submission 044153-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # R5970 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 52810934-52811495 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 52811322 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 57 (Y57H)
Ref Sequence ENSEMBL: ENSMUSP00000100423 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103646]
AlphaFold A0A075B642
Predicted Effect probably damaging
Transcript: ENSMUST00000103646
AA Change: Y57H

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000100423
Gene: ENSMUSG00000094792
AA Change: Y57H

IGv 40 114 1.33e-8 SMART
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.4%
Validation Efficiency 98% (63/64)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh1l1 G A 6: 90,597,046 (GRCm38) probably benign Het
Ambn T C 5: 88,467,951 (GRCm38) V413A possibly damaging Het
Amotl1 T A 9: 14,596,528 (GRCm38) D41V probably damaging Het
Arhgef26 T C 3: 62,340,047 (GRCm38) V184A probably benign Het
Birc6 G T 17: 74,618,502 (GRCm38) G936V possibly damaging Het
Ccser1 T A 6: 61,311,242 (GRCm38) S130T possibly damaging Het
Cecr2 A G 6: 120,720,907 (GRCm38) I56V probably damaging Het
Cfap52 A G 11: 67,930,744 (GRCm38) I486T probably damaging Het
Col4a3 A G 1: 82,716,329 (GRCm38) I1557V possibly damaging Het
Col6a5 T A 9: 105,945,847 (GRCm38) I104F unknown Het
Cry2 A G 2: 92,412,967 (GRCm38) S510P probably benign Het
Csmd2 G C 4: 128,546,151 (GRCm38) A3133P probably benign Het
Cyld G T 8: 88,732,993 (GRCm38) A611S probably damaging Het
Dennd4c G A 4: 86,825,512 (GRCm38) G1197E probably damaging Het
Dnah10 T C 5: 124,808,729 (GRCm38) F2969L probably benign Het
Dnaic1 A G 4: 41,625,281 (GRCm38) K415R probably benign Het
Dnmbp T A 19: 43,854,171 (GRCm38) T1253S probably benign Het
Dsp T C 13: 38,195,702 (GRCm38) L1542P possibly damaging Het
Duox1 T A 2: 122,340,201 (GRCm38) L1234Q probably damaging Het
Efr3b T A 12: 3,968,590 (GRCm38) R585S possibly damaging Het
Gpt A G 15: 76,699,352 (GRCm38) probably null Het
Heatr6 G A 11: 83,753,718 (GRCm38) probably benign Het
Kcns2 A G 15: 34,839,784 (GRCm38) D431G probably benign Het
Kdm3b A G 18: 34,829,289 (GRCm38) N1543D probably damaging Het
Man2a1 A G 17: 64,625,380 (GRCm38) K154R probably benign Het
Mical3 G A 6: 120,958,271 (GRCm38) Q893* probably null Het
Morc3 C T 16: 93,866,453 (GRCm38) H515Y possibly damaging Het
Mprip A T 11: 59,757,721 (GRCm38) R750S probably damaging Het
Mroh1 G A 15: 76,451,491 (GRCm38) V1436M probably benign Het
Muc5ac C T 7: 141,790,669 (GRCm38) R69* probably null Het
Muc5b A T 7: 141,856,712 (GRCm38) Y1274F unknown Het
Mybpc1 A G 10: 88,542,456 (GRCm38) L674P probably damaging Het
Mypn A G 10: 63,131,023 (GRCm38) V958A probably benign Het
Nipbl T C 15: 8,296,818 (GRCm38) T2436A probably benign Het
Olfr835 A G 9: 19,035,147 (GRCm38) D8G probably benign Het
Pcdhb5 T A 18: 37,321,773 (GRCm38) L402Q probably damaging Het
Pigp T A 16: 94,370,194 (GRCm38) probably null Het
Rp1 A G 1: 4,348,462 (GRCm38) L809P probably benign Het
Scn3a T A 2: 65,494,781 (GRCm38) probably benign Het
Sdf2 A T 11: 78,246,080 (GRCm38) M29L probably benign Het
Serpina3b T G 12: 104,134,091 (GRCm38) L311V possibly damaging Het
Snx31 A T 15: 36,523,488 (GRCm38) Y349* probably null Het
Spidr A C 16: 16,114,869 (GRCm38) C182W probably damaging Het
St13 A T 15: 81,377,798 (GRCm38) S146R probably damaging Het
St8sia4 A G 1: 95,653,582 (GRCm38) V145A probably damaging Het
Stradb T C 1: 58,980,016 (GRCm38) probably null Het
Tcp11l2 T A 10: 84,594,797 (GRCm38) probably benign Het
Tfdp2 C T 9: 96,317,574 (GRCm38) P74S unknown Het
Tmprss15 C T 16: 79,057,659 (GRCm38) R287H probably benign Het
Vmn2r104 A G 17: 20,029,471 (GRCm38) I846T probably benign Het
Ywhah T A 5: 33,026,948 (GRCm38) M165K possibly damaging Het
Zfp324 C A 7: 12,969,366 (GRCm38) P72T probably benign Het
Other mutations in Trav10d
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5378:Trav10d UTSW 14 52,811,368 (GRCm38) missense probably benign 0.01
R5898:Trav10d UTSW 14 52,811,472 (GRCm38) missense probably damaging 1.00
R8458:Trav10d UTSW 14 52,811,323 (GRCm38) missense probably damaging 1.00
R9410:Trav10d UTSW 14 52,811,388 (GRCm38) missense probably benign 0.00
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2017-03-31