Gene >> KRT37
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225550 |
| Start |
41422894:41422894(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.616G>A |
| AA Mutation |
p.Asp206Asn(p.D206N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225550 |
| Start |
41421403:41421403(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1205C>A |
| AA Mutation |
p.Ala402Asp(p.A402D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |