Variant #0000253195 (NC_000001.10:g.186277989A>G, NM_005807.3:c.3138A>G (PRG4))

Chromosome 1
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.186277989A>G
DNA change (hg38) g.186308857A>G
Published as PRG4(NM_005807.4):c.3138A>G (p.P1046=), PRG4(NM_005807.6):c.3138A>G (p.P1046=)
ISCN -
DB-ID PRG4_000021 See all 3 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) 0.3096 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
TPR NM_003292.2 -/. - c.*5114T>C r.(=) p.(=)
PRG4 NM_005807.3 -/. - c.3138A>G r.(?) p.(=)


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