| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308406 |
| Start |
19381392:19381392(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1183A>T |
| AA Mutation |
p.Ile395Phe(p.I395F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308406 |
| Start |
19382128:19382128(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1825C>T |
| AA Mutation |
p.Pro609Ser(p.P609S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308406 |
| Start |
19380815:19380815(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.606T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |