| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265713 |
| Start |
41978705:41978705(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.980T>C |
| AA Mutation |
p.Ile327Thr(p.I327T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265713 |
| Start |
41978699:41978699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.986G>A |
| AA Mutation |
p.Arg329Gln(p.R329Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265713 |
| Start |
41949255:41949255(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1707G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |