Variant #0000616102 (NC_000016.9:g.70208263G>T, NM_017990.3:c.*17481G>T (PDPR))

Chromosome 16
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.70208263G>T
DNA change (hg38) g.70174360G>T
Published as CLEC18C(NM_173619.3):c.82G>T (p.V28L)
ISCN -
DB-ID CLEC18C_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) 6.0E-5 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 2019-12-04 15:24:38 +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     
PDPR NM_017990.3 -?/. - c.*17481G>T r.(=) p.(=)
CLEC18C NM_173619.2 -?/. - c.82G>T r.(?) p.(Val28Leu)


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