Variant #0000324597 (NC_000016.9:g.11362728C>T, NM_021247.1:c.*4413G>A (PRM3))

Chromosome 16
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.11362728C>T
DNA change (hg38) g.11268871C>T
Published as TNP2(NM_005425.4):c.392G>A (p.(Arg131Gln))
ISCN -
DB-ID TNP2_000001
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) 0.00042 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNP2 NM_005425.4 ?/. - c.392G>A r.(?) p.(Arg131Gln)
PRM3 NM_021247.1 ?/. - c.*4413G>A r.(=) p.(=)


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