Variant #0001038466 (NC_000011.9:g.46726554G>A, NM_024741.2:c.1304G>A (ZNF408))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46726554G>A
DNA change (hg38) -
Published as ZNF408(NM_024741.2):c.1304G>A (p.R435Q), ZNF408(NM_024741.3):c.1304G>A (p.(Arg435Gln))
ISCN -
DB-ID ZNF408_000026 See all 5 reported entries
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) 0.00012 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 2025-05-05 21:14:00 +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     
ARHGAP1 NM_004308.3 ?/. - c.-4503C>T r.(?) p.(=)
ZNF408 NM_024741.2 ?/. - c.1304G>A r.(?) p.(Arg435Gln)


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