| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000622429 |
| Start |
74591775:74591775(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143528758
|
| CDS Mutation |
c.1381G>A |
| AA Mutation |
p.Ala461Thr(p.A461T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000622429 |
| Start |
74591351:74591351(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375732452
|
| CDS Mutation |
c.1082G>A |
| AA Mutation |
p.Arg361His(p.R361H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000622429 |
| Start |
74544468:74544468(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.532C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |