| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000167588 |
| Start |
40880135:40880135(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.757A>T |
| AA Mutation |
p.Asn253Tyr(p.N253Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000167588 |
| Start |
40878214:40878214(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1070T>C |
| AA Mutation |
p.Leu357Pro(p.L357P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000167588 |
| Start |
40879822:40879822(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.909T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |