Variant #0001002918 (NC_000017.10:g.12661420T>G, NM_014859.4:c.-31736T>G (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.12661420T>G
DNA change (hg38) -
Published as MYOCD(NM_001146312.1):c.2221T>G (p.(Ser741Ala))
ISCN -
DB-ID ARHGAP44_000023
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP44 NM_014859.4 -?/. - c.-31736T>G r.(?) p.(=)
MYOCD NM_153604.2 -?/. - c.2077T>G r.(?) p.(Ser693Ala)


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