Variant #0000544006 (NC_000011.9:g.46723022C>G, NM_024741.2:c.126C>G (ZNF408))

Chromosome 11
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.46723022C>G
DNA change (hg38) g.46701472C>G
Published as ZNF408(NM_001184751.1):c.102C>G (p.(Asp34Glu))
ISCN -
DB-ID ARHGAP1_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) 0.00061 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP1 NM_004308.3 -?/. - c.-971G>C r.(?) p.(=)
ZNF408 NM_024741.2 -?/. - c.126C>G r.(?) p.(Asp42Glu)


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