Variant #0000325122 (NC_000017.10:g.4451874A>C, NM_014520.3:c.1501T>G (MYBBP1A))

Chromosome 17
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.4451874A>C
DNA change (hg38) g.4548579A>C
Published as MYBBP1A(NM_001105538.1):c.1501T>G (p.(Phe501Val))
ISCN -
DB-ID MYBBP1A_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPNS2 NM_001124758.1 ?/. - c.*11131A>C r.(=) p.(=)
MYBBP1A NM_014520.3 ?/. - c.1501T>G r.(?) p.(Phe501Val)


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