Variant #0001070274 (NC_000022.10:g.30405084C>T, NM_021090.3:c.1087C>T (MTMR3))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.30405084C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MTMR3_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2517740814
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-10 11:44:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR3 NM_021090.3 ?/. - c.1087C>T r.(?) p.(Arg363Trp)


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