Variant #0000983178 (NC_000019.9:g.11306494C>A, NM_020812.3:c.*3679G>T (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.11306494C>A
DNA change (hg38) -
Published as KANK2(NM_001136191.3):c.-276G>T
ISCN -
DB-ID C19orf80_000086
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KANK2 NM_015493.6 -?/. - c.-1307G>T r.(?) p.(=)
C19orf80 NM_018687.6 -?/. - c.-43820C>A r.(?) p.(=)
DOCK6 NM_020812.3 -?/. - c.*3679G>T r.(=) p.(=)


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