Variant #0000163458 (NC_000016.9:g.16295943G>C, NM_001171.5:c.(1091C>G) (ABCC6))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.16295943G>C
DNA change (hg38) g.16202086G>C
Published as -
ISCN -
DB-ID ABCC6_000027 See all 4 reported entries
Variant remarks variant co-amplified from ABCC6P1 (scored as heterozygous)
Reference PubMed: Pulkkinen 2001
ClinVar ID -
dbSNP ID -
Origin Artefact
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-03-04 15:42:31 +01:00 (CET)
Date last edited 2020-07-14 22:02:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC6 NM_001171.5 ?/. 9 c.(1091C>G) r.(?) p.(Thr364Arg)


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