| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265801 |
| Start |
20254995:20254995(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.187G>A |
| AA Mutation |
p.Glu63Lys(p.E63K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265801 |
| Start |
20253247:20253247(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.684G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265801 |
| Start |
20255104:20255104(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.78C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |