| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000503731 |
| Start |
15650760:15650760(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779451208
|
| CDS Mutation |
c.372C>G |
| AA Mutation |
p.Asn124Lys(p.N124K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000503731 |
| Start |
15540437:15540437(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764280802
|
| CDS Mutation |
c.7G>T |
| AA Mutation |
p.Ala3Ser(p.A3S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000503731 |
| Start |
15623116:15623116(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.175T>C |
| AA Mutation |
p.Trp59Arg(p.W59R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |