| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249075 |
| Start |
30243991:30243991(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779219330
|
| CDS Mutation |
c.269C>T |
| AA Mutation |
p.Pro90Leu(p.P90L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000249075 |
| Start |
30243672:30243672(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201964524
|
| CDS Mutation |
c.588C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000249075 |
| Start |
30244899:30244899(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.54A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |