Variant #0000605766 (NC_000001.10:g.42925369C>T, NM_024664.2:c.708C>T (PPCS))

Chromosome 1
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.42925369C>T
DNA change (hg38) g.42459698C>T
Published as PPCS(NM_024664.4):c.708C>T (p.P236=)
ISCN -
DB-ID PPCS_000005
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) 0.00044 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 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPCS NM_024664.2 -?/. - c.708C>T r.(?) p.(Pro236=)
ZMYND12 NM_032257.4 -?/. - c.-3701G>A r.(?) p.(=)


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