| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358368 |
| Start |
7622592:7622592(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1441T>C |
| AA Mutation |
p.Tyr481His(p.Y481H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358368 |
| Start |
7622831:7622831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1302C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358368 |
| Start |
7622641:7622641(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1392C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |