Variant #0000622565 (NC_000011.9:g.118530637C>T, NM_001144758.2:c.*3104C>T (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.118530637C>T
DNA change (hg38) g.118659928C>T
Published as TREH(NM_007180.2):c.1139G>A (p.R380Q)
ISCN -
DB-ID TREH_000011
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) 0.00044 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 2019-12-06 12:43:26 +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.*3104C>T r.(=) p.(=)
TREH NM_007180.2 -?/. - c.1139G>A r.(?) p.(Arg380Gln)


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