| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000400314 |
| Start |
45909407:45909407(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753735130
|
| CDS Mutation |
c.392C>T |
| AA Mutation |
p.Thr131Met(p.T131M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000400314 |
| Start |
45935272:45935272(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs576585779
|
| CDS Mutation |
c.876G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000400314 |
| Start |
45911000:45911000(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774328273
|
| CDS Mutation |
c.570C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |