Gene >> NR2F1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327111 |
| Start |
93588064:93588064(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.611G>A |
| AA Mutation |
p.Gly204Asp(p.G204D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327111 |
| Start |
93588100:93588100(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.647T>C |
| AA Mutation |
p.Ile216Thr(p.I216T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |