Variant #0000140291 (NC_000016.9:g.16248934T>C, NC_000016.9(NM_001171.5):c.3883-46A>G (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.16248934T>C
DNA change (hg38) g.16155077T>C
Published as -
ISCN -
DB-ID ABCC6_000325 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs57745014
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00316 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 ?/. 27i c.3883-46A>G r.(=) p.(=)


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