Gene >> NOC2L
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327044 |
| Start |
953835:953835(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772311539
|
| CDS Mutation |
c.835G>A |
| AA Mutation |
p.Val279Met(p.V279M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327044 |
| Start |
944699:944699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747335515
|
| CDS Mutation |
c.2245G>A |
| AA Mutation |
p.Asp749Asn(p.D749N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |