Variant #0000300698 (NC_000004.11:g.186427772C>G, NM_014476.5:c.697G>C (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.186427772C>G
DNA change (hg38) g.185506618C>G
Published as PDLIM3(NM_014476.5):c.697G>C (p.V233L), PDLIM3(NM_014476.6):c.697G>C (p.V233L)
ISCN -
DB-ID PDLIM3_010009 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) 0.00042 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDLIM3 NM_014476.5 -?/. - c.697G>C r.(?) p.(Val233Leu)


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