Gene >> TNFRSF10B
| ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000276431 |
| Start |
23024258:23024258(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.939A>T |
| AA Mutation |
p.Glu313Asp(p.E313D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000276431 |
| Start |
23043136:23043136(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.250+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |