Variant #0001004334 (NC_000019.9:g.11314922G>A, NM_020812.3:c.5174C>T (DOCK6))

Chromosome 19
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.11314922G>A
DNA change (hg38) -
Published as DOCK6(NM_020812.3):c.5174C>T (p.(Ala1725Val))
ISCN -
DB-ID C19orf80_000095
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) 4.0E-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     
C19orf80 NM_018687.6 -?/. - c.-35392G>A r.(?) p.(=)
DOCK6 NM_020812.3 -?/. - c.5174C>T r.(?) p.(Ala1725Val)


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