Variant #0000852784 (NC_000011.9:g.118531377G>A, NM_001144758.2:c.*3844G>A (PHLDB1))

Chromosome 11
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.118531377G>A
DNA change (hg38) -
Published as TREH(NM_007180.2):c.973C>T (p.R325C)
ISCN -
DB-ID TREH_000014
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) 4.0E-5 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHLDB1 NM_001144758.2 ?/. - c.*3844G>A r.(=) p.(=)
TREH NM_007180.2 ?/. - c.973C>T r.(?) p.(Arg325Cys)


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