Variant #0001039506 (NC_000012.11:g.89866018T>C, NM_172240.2:c.487A>G (POC1B))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89866018T>C
DNA change (hg38) -
Published as POC1B(NM_172240.3):c.487A>G (p.(Ser163Gly))
ISCN -
DB-ID GALNT4_000021
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POC1B-GALNT4 NM_001199781.1 ?/. - c.*50572A>G r.(=) p.(=)
GALNT4 NM_003774.4 ?/. - c.*50572A>G r.(=) p.(=)
POC1B NM_172240.2 ?/. - c.487A>G r.(?) p.(Ser163Gly)


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