Variant #0000531090 (NC_000007.13:g.143882739A>C, NM_001003702.2:c.*1283T>G (ARHGEF35))

Chromosome 7
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.143882739A>C
DNA change (hg38) g.144185646A>C
Published as CTAGE4(NM_198495.2):c.2143A>C (p.M715L)
ISCN -
DB-ID ARHGEF35_000003
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 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.*1283T>G r.(=) p.(=)
CTAGE4 NM_198495.2 -?/. - c.2143A>C r.(?) p.(Met715Leu)


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