| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355305 |
| Start |
172131273:172131273(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1674G>C |
| AA Mutation |
p.Trp558Cys(p.W558C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000355305 |
| Start |
172387153:172387153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2097C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000355305 |
| Start |
172387291:172387291(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2235C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |