| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229971 |
| Start |
98926730:98926730(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.259A>C |
| AA Mutation |
p.Ser87Arg(p.S87R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229971 |
| Start |
98926928:98926928(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369518305
|
| CDS Mutation |
c.61C>T |
| AA Mutation |
p.Arg21Cys(p.R21C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229971 |
| Start |
98880608:98880608(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1334G>A |
| AA Mutation |
p.Ser445Asn(p.S445N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |