Variant #0000547606 (NC_000012.11:g.22078977A>G, NM_005691.2:c.305T>C (ABCC9))

Chromosome 12
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.22078977A>G
DNA change (hg38) g.21926043A>G
Published as ABCC9(NM_020297.2):c.305T>C (p.L102P), ABCC9(NM_020297.4):c.305T>C (p.L102P)
ISCN -
DB-ID ABCC9_000164 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) 9.0E-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 2019-07-18 18:22:55 +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.305T>C r.(?) p.(Leu102Pro)


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