Variant #0000320249 (NC_000011.9:g.46724598C>T, NM_024741.2:c.457C>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.46724598C>T
DNA change (hg38) g.46703048C>T
Published as ZNF408(NM_024741.2):c.457C>T (p.L153F)
ISCN -
DB-ID ZNF408_000006
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) 0.0003 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-2547G>A r.(?) p.(=)
ZNF408 NM_024741.2 ?/. - c.457C>T r.(?) p.(Leu153Phe)


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