| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309958 |
| Start |
51017126:51017126(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.253G>A |
| AA Mutation |
p.Ala85Thr(p.A85T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309958 |
| Start |
51017120:51017120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.259T>A |
| AA Mutation |
p.Cys87Ser(p.C87S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309958 |
| Start |
51017183:51017183(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.196G>T |
| AA Mutation |
p.Gly66Cys(p.G66C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |