Variant #0000312037 (NC_000011.9:g.118529017T>G, NM_001144758.2:c.*1484T>G (PHLDB1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.118529017T>G
DNA change (hg38) g.118658307=
Published as TREH(NM_007180.3):c.1734A>C (p.L578=)
ISCN -
DB-ID TREH_000004 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) 0.99994 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*1484T>G r.(=) p.(=)
TREH NM_007180.2 -/. - c.1734= r.(=) p.(Leu578=)


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