| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155172207:155172207(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2071G>T |
| AA Mutation |
p.Ala691Ser(p.A691S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155142055:155142055(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1022A>T |
| AA Mutation |
p.Glu341Val(p.E341V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155168569:155168569(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1858C>A |
| AA Mutation |
p.Gln620Lys(p.Q620K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |