| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000349533 |
| Start |
65636828:65636828(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3311T>A |
| AA Mutation |
p.Phe1104Tyr(p.F1104Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000349533 |
| Start |
65616065:65616065(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2053A>T |
| AA Mutation |
p.Thr685Ser(p.T685S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000349533 |
| Start |
65636499:65636499(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2982A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |