| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327858 |
| Start |
45550522:45550522(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1604A>G |
| AA Mutation |
p.Asn535Ser(p.N535S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327858 |
| Start |
45547128:45547128(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1365C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327858 |
| Start |
45541338:45541338(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1032C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |