Variant #0000565995 (NC_000019.9:g.11356356C>G, NM_020812.3:c.906G>C (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.11356356C>G
DNA change (hg38) g.11245680C>G
Published as DOCK6(NM_001367830.1):c.906G>C (p.S302=)
ISCN -
DB-ID C19orf80_000043
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) 0.00154 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 12:21:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf80 NM_018687.6 -?/. - c.*3993C>G r.(=) p.(=)
DOCK6 NM_020812.3 -?/. - c.906G>C r.(?) p.(Ser302=)


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