Variant #0000865840 (NC_000019.9:g.11311656C>T, NM_020812.3:c.5761G>A (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.11311656C>T
DNA change (hg38) -
Published as DOCK6(NM_020812.3):c.5761G>A (p.(Glu1921Lys))
ISCN -
DB-ID C19orf80_000064
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KANK2 NM_015493.6 -?/. - c.-6469G>A r.(?) p.(=)
C19orf80 NM_018687.6 -?/. - c.-38658C>T r.(?) p.(=)
DOCK6 NM_020812.3 -?/. - c.5761G>A r.(?) p.(Glu1921Lys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.