Variant #0000998802 (NC_000011.9:g.118532376A>G, NM_001144758.2:c.*4843A>G (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.118532376A>G
DNA change (hg38) -
Published as TREH(NM_007180.2):c.587T>C (p.(Met196Thr))
ISCN -
DB-ID TREH_000016
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) 0.00438 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHLDB1 NM_001144758.2 ?/. - c.*4843A>G r.(=) p.(=)
TREH NM_007180.2 ?/. - c.587T>C r.(?) p.?


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