| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377086 |
| Start |
10352685:10352685(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4004C>T |
| AA Mutation |
p.Ser1335Phe(p.S1335F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377086 |
| Start |
10348684:10348684(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3900T>A |
| AA Mutation |
p.His1300Gln(p.H1300Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377086 |
| Start |
10348664:10348664(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3880A>T |
| AA Mutation |
p.Ile1294Phe(p.I1294F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |