Variant #0001002374 (NC_000016.9:g.4752125_4752127del, NM_139170.2:c.-32626_-32624del (C16orf71))

Chromosome 16
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.4752125_4752127del
DNA change (hg38) -
Published as ANKS3(NM_133450.3):c.1002_1004delCAG (p.(Ser335del))
ISCN -
DB-ID ANKS3_000022
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 2024-08-28 13:16:32 +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     
ANKS3 NM_133450.3 -?/. - c.1002_1004del r.(?) p.(Ser335del)
C16orf71 NM_139170.2 -?/. - c.-32626_-32624del r.(?) p.(=)


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