Gene >> MSH5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375750 |
| Start |
31758856:31758856(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1307G>A |
| AA Mutation |
p.Ser436Asn(p.S436N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000375750 |
| Start |
31758873:31758873(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1324C>G |
| AA Mutation |
p.Leu442Val(p.L442V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |