Variant #0000294073 (NC_000012.11:g.89814934C>A, NM_172240.2:c.1433G>T (POC1B))

Chromosome 12
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.89814934C>A
DNA change (hg38) g.89421157C>A
Published as POC1B(NM_172240.3):c.1433G>T (p.S478I)
ISCN -
DB-ID POC1B_000003 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) 0.00081 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POC1B-GALNT4 NM_001199781.1 -?/. - c.*101656G>T r.(=) p.(=)
GALNT4 NM_003774.4 -?/. - c.*101656G>T r.(=) p.(=)
POC1B NM_172240.2 -?/. - c.1433G>T r.(?) p.(Ser478Ile)


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