Variant #0000132645 (NC_000012.11:g.28122384A>C, NM_198965.1:c.44T>G (PTHLH))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.28122384A>C
DNA change (hg38) g.27969451A>C
Published as -
ISCN -
DB-ID PTHLH_000006 See all 2 reported entries
Variant remarks cDNA expression cloning in HEK293 cells shows affected signal peptide cleavage
Reference PubMed: Wang 2015
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-08-24 19:25:11 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTHLH NM_198965.1 +/+? 3 c.44T>G r.(?) p.Leu15Arg


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