Variant #0000980803 (NC_000014.8:g.21542939G>A, NM_001101672.1:c.*15756C>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.21542939G>A
DNA change (hg38) -
Published as ARHGEF40(NM_018071.5):c.1050G>A (p.(Leu350=))
ISCN -
DB-ID NDRG2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNASE13 NM_001012264.3 -?/. - c.-40133C>T r.(?) p.(=)
ZNF219 NM_001101672.1 -?/. - c.*15756C>T r.(=) p.(=)
NDRG2 NM_016250.2 -?/. - c.-49177C>T r.(?) p.(=)
RNASE7 NM_032572.3 -?/. - c.*31317G>A r.(=) p.(=)
RNASE8 NM_138331.1 -?/. - c.*16423G>A r.(=) p.(=)
TPPP2 NM_173846.4 -?/. - c.*42703G>A r.(=) p.(=)


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