| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000307128 |
| Start |
119186060:119186060(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.655T>G |
| AA Mutation |
p.Phe219Val(p.F219V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000307128 |
| Start |
119150940:119150940(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.145C>T |
| AA Mutation |
p.His49Tyr(p.H49Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000307128 |
| Start |
119186049:119186049(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.644C>T |
| AA Mutation |
p.Thr215Ile(p.T215I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |