| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319715 |
| Start |
24570301:24570301(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760684099
|
| CDS Mutation |
c.3611C>T |
| AA Mutation |
p.Ala1204Val(p.A1204V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319715 |
| Start |
24568849:24568849(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2159G>T |
| AA Mutation |
p.Ser720Ile(p.S720I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000319715 |
| Start |
24570158:24570158(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760944143
|
| CDS Mutation |
c.3468A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |