Variant #0000893007 (NC_000016.9:g.4748033C>G, NM_139170.2:c.-36718C>G (C16orf71))

Chromosome 16
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.4748033C>G
DNA change (hg38) -
Published as ANKS3(NM_133450.4):c.1755G>C (p.V585=)
ISCN -
DB-ID ANKS3_000010
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) 0.00341 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUDT16L1 NM_032349.3 -/. - c.*2853C>G r.(=) p.(=)
ANKS3 NM_133450.3 -/. - c.1755G>C r.(?) p.(Val585=)
C16orf71 NM_139170.2 -/. - c.-36718C>G r.(?) p.(=)


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