Variant #0000531096 (NC_000007.13:g.143884941T>C, NM_001003702.2:c.536A>G (ARHGEF35))

Chromosome 7
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.143884941T>C
DNA change (hg38) g.144187848T>C
Published as ARHGEF35(NM_001003702.2):c.536A>G (p.Q179R)
ISCN -
DB-ID ARHGEF35_000009
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) 0.00075 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 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     
ARHGEF35 NM_001003702.2 ?/. - c.536A>G r.(?) p.(Gln179Arg)
CTAGE4 NM_198495.2 ?/. - c.*2011T>C r.(=) p.(=)


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