| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265304 |
| Start |
141743911:141743911(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.236G>A |
| AA Mutation |
p.Ser79Asn(p.S79N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265304 |
| Start |
141743690:141743690(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200664859
|
| CDS Mutation |
c.215T>C |
| AA Mutation |
p.Val72Ala(p.V72A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265304 |
| Start |
141743577:141743577(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779739037
|
| CDS Mutation |
c.102C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |