Variant #0000267492 (NC_000019.9:g.11313256G>A, NC_000019.9(NM_020812.3):c.5361+4C>T (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.11313256G>A
DNA change (hg38) g.11202580G>A
Published as DOCK6(NM_020812.4):c.5361+4C>T
ISCN -
DB-ID DOCK6_000039 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) 0.39474 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 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.-37058G>A r.(?) p.(=)
DOCK6 NM_020812.3 -/. - c.5361+4C>T r.spl? p.?


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