| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000394945 |
| Start |
136988535:136988535(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.815T>A |
| AA Mutation |
p.Ile272Asn(p.I272N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394945 |
| Start |
136978687:136978687(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1287T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394945 |
| Start |
137140630:137140630(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.297C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |