| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360534 |
| Start |
162011838:162011838(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1787G>C |
| AA Mutation |
p.Arg596Thr(p.R596T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360534 |
| Start |
162016777:162016777(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1558A>T |
| AA Mutation |
p.Asn520Tyr(p.N520Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360534 |
| Start |
162018790:162018790(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1359G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |