| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377110 |
| Start |
71121288:71121288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.67T>A |
| AA Mutation |
p.Trp23Arg(p.W23R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377110 |
| Start |
70598499:70598499(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2932A>T |
| AA Mutation |
p.Ile978Phe(p.I978F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377110 |
| Start |
70862926:70862926(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.444C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |