| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265071 |
| Start |
31322847:31322847(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1912C>T |
| AA Mutation |
p.Arg638Trp(p.R638W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265071 |
| Start |
31323192:31323192(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2257C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265071 |
| Start |
31297377:31297377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.612A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |