Variant #0000609162 (NC_000004.11:g.186446257G>A, NM_014476.5:c.162C>T (PDLIM3))

Chromosome 4
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.186446257G>A
DNA change (hg38) g.185525103G>A
Published as PDLIM3(NM_014476.5):c.162C>T (p.G54=), PDLIM3(NM_014476.6):c.162C>T (p.G54=)
ISCN -
DB-ID PDLIM3_000007 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) 0.00796 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDLIM3 NM_014476.5 -?/. - c.162C>T r.(?) p.(Gly54=)


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