| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330843 |
| Start |
37874833:37874833(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1304C>A |
| AA Mutation |
p.Ser435Tyr(p.S435Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330843 |
| Start |
37871396:37871396(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3406G>T |
| AA Mutation |
p.Ala1136Ser(p.A1136S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000330843 |
| Start |
37874949:37874949(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780045862
|
| CDS Mutation |
c.1188G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |