| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315576 |
| Start |
14764479:14764479(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1038G>T |
| AA Mutation |
p.Lys346Asn(p.K346N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315576 |
| Start |
14751547:14751547(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1913G>C |
| AA Mutation |
p.Ser638Thr(p.S638T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315576 |
| Start |
14756281:14756281(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1149G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |