| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000421745 |
| Start |
32515633:32515633(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.11212G>A |
| AA Mutation |
p.Ala3738Thr(p.A3738T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000421745 |
| Start |
32357241:32357241(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.80G>A |
| AA Mutation |
p.Arg27Gln(p.R27Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000421745 |
| Start |
32549427:32549427(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.13090C>T |
| AA Mutation |
p.Leu4364Phe(p.L4364F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |