Gene >> TRPV4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261740 |
| Start |
109800699:109800699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.772G>T |
| AA Mutation |
p.Val258Leu(p.V258L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261740 |
| Start |
109792722:109792722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1754G>T |
| AA Mutation |
p.Gly585Val(p.G585V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |