Variant #0000723455 (NC_000011.9:g.46726153G>T, NM_024741.2:c.903G>T (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.46726153G>T
DNA change (hg38) -
Published as ZNF408(NM_024741.2):c.903G>T (p.P301=), ZNF408(NM_024741.3):c.903G>T (p.P301=)
ISCN -
DB-ID ARHGAP1_000006 See all 2 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) 0.00018 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 2021-02-08 18:36:18 +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.-4102C>A r.(?) p.(=)
ZNF408 NM_024741.2 -?/. - c.903G>T r.(?) p.(Pro301=)


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