Variant #0000245355 (NC_000001.10:g.155113104G>T, NM_018973.3:c.-298C>A (DPM3))

Chromosome 1
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.155113104G>T
DNA change (hg38) g.155140628G>T
Published as -
ISCN -
DB-ID DPM3_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs4971073
Origin Germline
Segregation -
Frequency 0.14-0.92
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-04-16 20:05:12 +02:00 (CEST)
Date last edited 2018-01-14 21:40:10 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPM3 NM_018973.3 ?/. - c.-298C>A r.(?) p.(=)


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