Variant #0000248929 (NC_000001.10:g.186276661A>G, NM_005807.3:c.1810A>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.186276661A>G
DNA change (hg38) g.186307529A>G
Published as PRG4(NM_005807.6):c.1810A>G (p.T604A)
ISCN -
DB-ID PRG4_000018
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) 0.31179 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 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.*6442T>C r.(=) p.(=)
PRG4 NM_005807.3 -/. - c.1810A>G r.(?) p.(Thr604Ala)


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