Variant #0000569901 (NC_000020.10:g.47630449C>T, NM_006420.2:c.4131C>T (ARFGEF2))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47630449C>T
DNA change (hg38) g.49013912C>T
Published as ARFGEF2(NM_006420.2):c.4131C>T (p.I1377=), ARFGEF2(NM_006420.3):c.4131C>T (p.I1377=)
ISCN -
DB-ID ARFGEF2_000068 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) 0.19785 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
ARFGEF2 NM_006420.2 -/. - c.4131C>T r.(?) p.(Ile1377=)


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