Gene >> LAMA4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000230538 |
| Start |
112114104:112114104(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.5298G>C |
| AA Mutation |
p.Arg1766Ser(p.R1766S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000230538 |
| Start |
112109478:112109478(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5431G>A |
| AA Mutation |
p.Val1811Ile(p.V1811I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |