| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264501 |
| Start |
122356683:122356683(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.14563G>A |
| AA Mutation |
p.Val4855Met(p.V4855M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264501 |
| Start |
122243050:122243050(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4724T>G |
| AA Mutation |
p.Leu1575Arg(p.L1575R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264501 |
| Start |
122247236:122247236(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5391G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |