Gene >> MME
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155118749:155118749(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.658G>A |
| AA Mutation |
p.Asp220Asn(p.D220N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155140262:155140262(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.927A>C |
| AA Mutation |
p.Gln309His(p.Q309H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |