| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380872 |
| Start |
4965927:4965927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.98A>C |
| AA Mutation |
p.Lys33Thr(p.K33T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380872 |
| Start |
4966000:4966000(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763761256
|
| CDS Mutation |
c.171T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380872 |
| Start |
4972695:4972695(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.792G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |