| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291688 |
| Start |
46246817:46246817(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4360A>T |
| AA Mutation |
p.Ser1454Cys(p.S1454C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000291688 |
| Start |
46275231:46275231(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1953C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000291688 |
| Start |
46236910:46236910(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5703C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |