Variant #0000862945 (NC_000012.11:g.22068620A>G, NM_005691.2:c.798T>C (ABCC9))

Chromosome 12
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.22068620A>G
DNA change (hg38) -
Published as ABCC9(NM_005691.2):c.798T>C (p.(Asp266=)), ABCC9(NM_020297.4):c.798T>C (p.D266=)
ISCN -
DB-ID ABCC9_000155 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) 0.00027 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC9 NM_005691.2 -?/. - c.798T>C r.(?) p.(Asp266=)


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