Variant #0000514515 (NC_000002.11:g.216946353G>C, NM_018441.5:c.112C>G (PECR))

Chromosome 2
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.216946353G>C
DNA change (hg38) g.216081630G>C
Published as PECR(NM_018441.6):c.112C>G (p.(Leu38Val), p.L38V)
ISCN -
DB-ID PECR_000003 See all 2 reported entries
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) 0.00015 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PECR NM_018441.5 ?/. - c.112C>G r.(?) p.(Leu38Val)
TMEM169 NM_138390.3 ?/. - c.-472G>C r.(?) p.(=)


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