Variant #0000306237 (NC_000001.10:g.161139744T>C, NM_000309.3:c.917T>C (PPOX))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.161139744T>C
DNA change (hg38) g.161169954T>C
Published as PPOX(NM_000309.4):c.917T>C (p.L306P)
ISCN -
DB-ID PPOX_000009
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) Retrieve
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 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     
PPOX NM_000309.3 +?/. - c.917T>C r.(?) p.(Leu306Pro)
USP21 NM_001014443.2 +?/. - c.*4507T>C r.(=) p.(=)
B4GALT3 NM_003779.3 +?/. - c.*1862A>G r.(=) p.(=)


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