Gene >> NGFR
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000172229 |
| Start |
49510579:49510579(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.736G>C |
| AA Mutation |
p.Gly246Arg(p.G246R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000172229 |
| Start |
49512706:49512706(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.983-2A>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |