Variant #0000680778 (NC_000017.10:g.12659790C>T, NM_014859.4:c.-33366C>T (ARHGAP44))

Chromosome 17
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.12659790C>T
DNA change (hg38) -
Published as MYOCD(NM_001146312.2):c.2118C>T (p.H706=)
ISCN -
DB-ID ARHGAP44_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) 0.00425 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP44 NM_014859.4 -?/. - c.-33366C>T r.(?) p.(=)
MYOCD NM_153604.2 -?/. - c.2059-1612C>T r.(=) p.(=)


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