| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263645 |
| Start |
2394139:2394139(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.226G>C |
| AA Mutation |
p.Gly76Arg(p.G76R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263645 |
| Start |
2396858:2396858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.703G>A |
| AA Mutation |
p.Val235Met(p.V235M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263645 |
| Start |
2396680:2396680(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.614T>A |
| AA Mutation |
p.Ile205Asn(p.I205N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |