Variant #0000999048 (NC_000011.9:g.46726595C>T, NM_024741.2:c.1345C>T (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.46726595C>T
DNA change (hg38) -
Published as ZNF408(NM_001184751.1):c.1321C>T (p.(Gln441*))
ISCN -
DB-ID ARHGAP1_000024
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) 2.0E-5 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 2024-08-28 13:16:32 +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.-4544G>A r.(?) p.(=)
ZNF408 NM_024741.2 ?/. - c.1345C>T r.(?) p.(Arg449Trp)


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