Variant #0000558269 (NC_000016.9:g.4764086C>T, NM_139170.2:c.-20665C>T (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.4764086C>T
DNA change (hg38) g.4714085C>T
Published as ANKS3(NM_133450.4):c.675G>A (p.S225=)
ISCN -
DB-ID ANKS3_000004
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) 0.00015 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKS3 NM_133450.3 -?/. - c.675G>A r.(?) p.(Ser225=)
C16orf71 NM_139170.2 -?/. - c.-20665C>T r.(?) p.(=)


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