Variant #0000616342 (NC_000017.10:g.12666834C>T, NM_014859.4:c.-26322C>T (ARHGAP44))

Chromosome 17
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.12666834C>T
DNA change (hg38) g.12763517C>T
Published as MYOCD(NM_001146312.2):c.2834C>T (p.P945L)
ISCN -
DB-ID ARHGAP44_000002
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) 6.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
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     
ARHGAP44 NM_014859.4 ?/. - c.-26322C>T r.(?) p.(=)
MYOCD NM_153604.2 ?/. - c.2690C>T r.(?) p.(Pro897Leu)


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