Variant #0000522590 (NC_000004.11:g.435522T>C, NC_000004.11(NR_002451.2):n.357-14760A>G (ABCA11P))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.435522T>C
DNA change (hg38) g.441733T>C
Published as ZNF721(NM_133474.4):c.2734A>G (p.K912E)
ISCN -
DB-ID ABCA11P_000003
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) 0.00011 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF721 NM_133474.2 -?/. - c.2734A>G r.(?) p.(Lys912Glu)
ABCA11P NR_002451.2 -?/. - n.357-14760A>G r.(?) -


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