Variant #0000522247 (NC_000004.11:g.186435435C>T, NM_014476.5:c.387G>A (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.186435435C>T
DNA change (hg38) g.185514281C>T
Published as PDLIM3(NM_014476.5):c.387G>A (p.P129=), PDLIM3(NM_014476.6):c.387G>A (p.P129=)
ISCN -
DB-ID PDLIM3_000009 See all 3 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) 0.00147 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 2019-07-18 18:22:55 +02:00 (CEST)
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.387G>A r.(?) p.(Pro129=)


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