Variant #0000248711 (NC_000019.9:g.11311109A>T, NM_020812.3:c.5976T>A (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.11311109A>T
DNA change (hg38) g.11200433A>T
Published as DOCK6(NM_020812.4):c.5976T>A (p.I1992=)
ISCN -
DB-ID DOCK6_000035
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) 0.00201 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-5922T>A r.(?) p.(=)
C19orf80 NM_018687.6 -/. - c.-39205A>T r.(?) p.(=)
DOCK6 NM_020812.3 -/. - c.5976T>A r.(?) p.(Ile1992=)


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