Variant #0000311451 (NC_000011.9:g.46723095C>G, NM_024741.2:c.199C>G (ZNF408))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46723095C>G
DNA change (hg38) g.46701545C>G
Published as ZNF408(NM_024741.3):c.199C>G (p.L67V)
ISCN -
DB-ID ZNF408_000004
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) 0.00079 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-1044G>C r.(?) p.(=)
ZNF408 NM_024741.2 -/. - c.199C>G r.(?) p.(Leu67Val)


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