Variant #0000522594 (NC_000004.11:g.435957G>T, ABCA11P(NR_002451.2):n.357-15195C>A)

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.435957G>T
DNA change (hg38) g.442168G>T
Published as ZNF721(NM_133474.4):c.2299C>A (p.H767N)
ISCN -
DB-ID ABCA11P_000007
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF721 NM_133474.2 -?/. - c.2299C>A r.(?) p.(His767Asn)
ABCA11P NR_002451.2 -?/. - n.357-15195C>A r.(?) -