Variant #0000963672 (NC_000005.9:g.70936845G>A, NM_022132.4:c.1015G>A (MCCC2))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70936845G>A
DNA change (hg38) -
Published as MCCC2(NM_022132.4):c.1015G>A (p.V339M), MCCC2(NM_022132.5):c.1015G>A (p.(Val339Met), p.V339M)
ISCN -
DB-ID MCCC2_000003 See all 8 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0008 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCCC2 NM_022132.4 +/. - c.1015G>A r.(?) p.(Val339Met)


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