Gene >> TCF7
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342854 |
| Start |
134142869:134142869(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.904A>T |
| AA Mutation |
p.Ile302Phe(p.I302F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342854 |
| Start |
134138107:134138107(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775076567
|
| CDS Mutation |
c.490G>A |
| AA Mutation |
p.Glu164Lys(p.E164K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |