Variant #0000140144 (NC_000016.9:g.16272792G>A, NM_001171.5:c.2278C>T (ABCC6))

Chromosome 16
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.16272792G>A
DNA change (hg38) g.16178935G>A
Published as -
ISCN -
DB-ID ABCC6_000082 See all 8 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72653788
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Tim Hefferon
Database submission license No license selected
Created by Tim Hefferon
Date created 2013-02-16 00:10:40 +01:00 (CET)
Date last edited 2021-09-09 14:48:34 +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 ?/. 18 c.2278C>T r.(?) p.(Arg760Trp)


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