| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000616054 |
| Start |
36064388:36064388(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.46G>A |
| AA Mutation |
p.Ala16Thr(p.A16T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000616054 |
| Start |
36064388:36064388(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.46G>T |
| AA Mutation |
p.Ala16Ser(p.A16S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000616054 |
| Start |
36071037:36071037(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.266C>T |
| AA Mutation |
p.Ala89Val(p.A89V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |