Variant #0000658742 (NC_000020.10:g.31620843G>T, NM_174897.2:c.151G>T (BPIFB6))

Chromosome 20
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.31620843G>T
DNA change (hg38) g.33033037G>T
Published as BPIFB6(NM_174897.2):c.151G>T (p.(Ala51Ser))
ISCN -
DB-ID BPIFB6_000003
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) 4.0E-5 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 2020-03-23 16:13:27 +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     
BPIFB6 NM_174897.2 ?/. - c.151G>T r.(?) p.(Ala51Ser)


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