Variant #0000551484 (NC_000014.8:g.21542965G>A, NM_001101672.1:c.*15730C>T (ZNF219))

Chromosome 14
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.21542965G>A
DNA change (hg38) g.21074806G>A
Published as ARHGEF40(NM_018071.4):c.1076G>A (p.G359E)
ISCN -
DB-ID NDRG2_000001
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) Retrieve
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     
RNASE13 NM_001012264.3 -?/. - c.-40159C>T r.(?) p.(=)
ZNF219 NM_001101672.1 -?/. - c.*15730C>T r.(=) p.(=)
NDRG2 NM_016250.2 -?/. - c.-49203C>T r.(?) p.(=)
ARHGEF40 NM_018071.3 -?/. - c.1076G>A r.(?) p.(Gly359Glu)
RNASE7 NM_032572.3 -?/. - c.*31343G>A r.(=) p.(=)
RNASE8 NM_138331.1 -?/. - c.*16449G>A r.(=) p.(=)
TPPP2 NM_173846.4 -?/. - c.*42729G>A r.(=) p.(=)


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