Variant #0000719993 (NC_000004.11:g.77134617C>T, NM_001204255.1:c.80G>A (SCARB2))

Chromosome 4
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.77134617C>T
DNA change (hg38) -
Published as SCARB2(NM_005506.3):c.80G>A (p.R27Q)
ISCN -
DB-ID SCARB2_000004 See all 2 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) 0.00016 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM47E NM_001136570.2 ?/. - c.-38283C>T r.(?) p.(=)
SCARB2 NM_001204255.1 ?/. - c.80G>A r.(?) p.(Arg27Gln)
FAM47E-STBD1 NM_001242939.1 ?/. - c.-38283C>T r.(?) p.(=)


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