| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000394836 |
| Start |
61908106:61908106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.212T>A |
| AA Mutation |
p.Ile71Asn(p.I71N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394836 |
| Start |
61908060:61908060(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs759926846
|
| CDS Mutation |
c.258G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394836 |
| Start |
61904620:61904620(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750620646
|
| CDS Mutation |
c.825G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |