Variant #0000868115 (NC_000008.10:g.144297084C>T, NC_000008.10(NM_178172.3):c.296-50C>T (GPIHBP1))

Chromosome 8
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.144297084C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GPIHBP1_000097
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs78632677
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00137 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-05-11 14:33:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPIHBP1 NM_178172.3 ?/. - c.296-50C>T r.(?) p.(?)


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