| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339562 |
| Start |
156325913:156325913(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775615135
|
| CDS Mutation |
c.1628A>G |
| AA Mutation |
p.Asn543Ser(p.N543S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339562 |
| Start |
156329973:156329973(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.214G>A |
| AA Mutation |
p.Asp72Asn(p.D72N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000339562 |
| Start |
156329830:156329830(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.357G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |