Variant #0000562283 (NC_000017.10:g.48736714A>G, NM_001144070.1:c.791A>G (ABCC3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48736714A>G
DNA change (hg38) g.50659353A>G
Published as ABCC3(NM_001144070.1):c.791A>G (p.(Glu264Gly)), ABCC3(NM_003786.4):c.791A>G (p.E264G)
ISCN -
DB-ID ABCC3_000001 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC3 NM_001144070.1 -?/. - c.791A>G r.(?) p.(Glu264Gly)


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