Variant #0000140165 (NC_000016.9:g.16271357delC, NM_001171.5:c.2542delG (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.16271357delC
DNA change (hg38) g.16177500delC
Published as -
ISCN -
DB-ID ABCC6_000101 See all 31 reported entries
Variant remarks Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID rs67867306
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC6 NM_001171.5 ?/. 19 c.2542delG r.(?) p.?


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