Variant #0000565931 (NC_000019.9:g.11311390A>G, NC_000019.9(NM_020812.3):c.5939+2T>C (DOCK6))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.11311390A>G
DNA change (hg38) g.11200714A>G
Published as DOCK6(NM_001367830.1):c.6044+2T>C, DOCK6(NM_020812.4):c.5939+2T>C
ISCN -
DB-ID DOCK6_000013 See all 5 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) 0.00021 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KANK2 NM_015493.6 +/. - c.-6203T>C r.(?) p.(=)
C19orf80 NM_018687.6 +/. - c.-38924A>G r.(?) p.(=)
DOCK6 NM_020812.3 +/. - c.5939+2T>C r.spl? p.?


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