Variant #0000565961 (NC_000019.9:g.11327608T>C, NM_020812.3:c.3876A>G (DOCK6))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11327608T>C
DNA change (hg38) g.11216932T>C
Published as DOCK6(NM_020812.4):c.3876A>G (p.L1292=)
ISCN -
DB-ID C19orf80_000020 See all 2 reported entries
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) 0.64568 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf80 NM_018687.6 -/. - c.-22706T>C r.(?) p.(=)
DOCK6 NM_020812.3 -/. - c.3876A>G r.(?) p.(Leu1292=)


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