Variant #0000976283 (NC_000004.11:g.3502057C>T, NM_173660.4:c.*6829C>T (DOK7))

Chromosome 4
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.3502057C>T
DNA change (hg38) -
Published as DOK7(NM_001301071.1):c.1620C>T (p.(Pro540=))
ISCN -
DB-ID DOK7_000203
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) 0.00914 View details
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     
LRPAP1 NM_002337.3 -?/. - c.*12644G>A r.(=) p.(=)
DOK7 NM_173660.4 -?/. - c.*6829C>T r.(=) p.(=)


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