| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000271452 |
| Start |
163355408:163355408(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755556279
|
| CDS Mutation |
c.1334A>G |
| AA Mutation |
p.Tyr445Cys(p.Y445C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000271452 |
| Start |
163326090:163326090(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.39G>C |
| AA Mutation |
p.Glu13Asp(p.E13D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000271452 |
| Start |
163348974:163348974(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1154G>A |
| AA Mutation |
p.Gly385Asp(p.G385D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |