Variant #0000565986 (NC_000019.9:g.11347489C>T, NM_020812.3:c.2140G>A (DOCK6))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11347489C>T
DNA change (hg38) g.11236813C>T
Published as DOCK6(NM_020812.3):c.2140G>A (p.V714M, p.(Val714Met))
ISCN -
DB-ID C19orf80_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) 0.00092 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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf80 NM_018687.6 ?/. - c.-2825C>T r.(?) p.(=)
DOCK6 NM_020812.3 ?/. - c.2140G>A r.(?) p.(Val714Met)


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