Variant #0000723253 (NC_000011.9:g.118530495A>G, NM_001144758.2:c.*2962A>G (PHLDB1))

Chromosome 11
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.118530495A>G
DNA change (hg38) -
Published as TREH(NM_007180.2):c.1281T>C (p.S427=)
ISCN -
DB-ID TREH_000013
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.*2962A>G r.(=) p.(=)
TREH NM_007180.2 -?/. - c.1281T>C r.(?) p.(Ser427=)


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