| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327365 |
| Start |
24233921:24233921(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.257T>A |
| AA Mutation |
p.Met86Lys(p.M86K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327365 |
| Start |
24233927:24233927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.251A>T |
| AA Mutation |
p.Gln84Leu(p.Q84L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327365 |
| Start |
24232945:24232945(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.474C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |