Variant #0000321091 (NC_000001.10:g.161017765G>A, NM_181720.2:c.2413C>T (ARHGAP30))

Chromosome 1
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.161017765G>A
DNA change (hg38) g.161047975G>A
Published as ARHGAP30(NM_001025598.1):c.3046C>T (p.(Arg1016Trp))
ISCN -
DB-ID ARHGAP30_000001
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) 0.00472 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USF1 NM_007122.3 ?/. - c.-2203C>T r.(?) p.(=)
ARHGAP30 NM_181720.2 ?/. - c.2413C>T r.(?) p.(Arg805Trp)


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