| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305958 |
| Start |
4175246:4175246(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.191T>C |
| AA Mutation |
p.Val64Ala(p.V64A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305958 |
| Start |
4182740:4182740(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1261G>T |
| AA Mutation |
p.Gly421Cys(p.G421C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305958 |
| Start |
4187392:4187392(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1653C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |