| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357424 |
| Start |
48964324:48964324(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.243G>C |
| AA Mutation |
p.Lys81Asn(p.K81N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357424 |
| Start |
48964373:48964373(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370580614
|
| CDS Mutation |
c.194T>C |
| AA Mutation |
p.Met65Thr(p.M65T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357424 |
| Start |
48961792:48961792(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.285G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |