| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264657 |
| Start |
42322464:42322464(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769031989
|
| CDS Mutation |
c.1919A>T |
| AA Mutation |
p.Tyr640Phe(p.Y640F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264657 |
| Start |
42348434:42348434(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.83T>A |
| AA Mutation |
p.Met28Lys(p.M28K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264657 |
| Start |
42329558:42329558(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1229A>G |
| AA Mutation |
p.His410Arg(p.H410R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |