Variant #0000248368 (NC_000008.10:g.1808256A>G, NM_014629.2:c.387A>G (ARHGEF10))

Chromosome 8
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.1808256A>G
DNA change (hg38) g.1860090A>G
Published as ARHGEF10(NM_001308153.2):c.459A>G (p.V153=), ARHGEF10(NM_014629.4):c.387A>G (p.V129=)
ISCN -
DB-ID ARHGEF10_000007 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) 0.06073 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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     
ARHGEF10 NM_014629.2 -/. - c.387A>G r.(?) p.(Val129=)


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