Variant #0000261709 (NC_000012.11:g.22065975C>T, NM_005691.2:c.842G>A (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.22065975C>T
DNA change (hg38) g.21913041C>T
Published as ABCC9(NM_005691.2):c.842G>A (p.R281Q), ABCC9(NM_020297.2):c.842G>A (p.R281Q)
ISCN -
DB-ID ABCC9_000144 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +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.842G>A r.(?) p.(Arg281Gln)


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