| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000618040 |
| Start |
154772089:154772089(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1334T>C |
| AA Mutation |
p.Phe445Ser(p.F445S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000618040 |
| Start |
154869585:154869585(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.380G>A |
| AA Mutation |
p.Gly127Asp(p.G127D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000618040 |
| Start |
154869619:154869619(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.346T>A |
| AA Mutation |
p.Ser116Thr(p.S116T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |