| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339562 |
| Start |
156329789:156329789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.398C>T |
| AA Mutation |
p.Pro133Leu(p.P133L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339562 |
| Start |
156329726:156329726(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.461A>T |
| AA Mutation |
p.Gln154Leu(p.Q154L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339562 |
| Start |
156330147:156330147(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.40G>A |
| AA Mutation |
p.Gly14Arg(p.G14R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |