Variant #0000325125 (NC_000017.10:g.4457215G>C, NC_000017.10(NM_014520.3):c.454-3C>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.4457215G>C
DNA change (hg38) g.4553920G>C
Published as MYBBP1A(NM_001105538.1):c.454-3C>G (p.?)
ISCN -
DB-ID MYBBP1A_000007
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 2020-07-11 13:38:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPNS2 NM_001124758.1 ?/. - c.*16472G>C r.(=) p.(=)
MYBBP1A NM_014520.3 ?/. - c.454-3C>G r.spl? p.?
GGT6 NM_153338.2 ?/. - c.*4095C>G r.(=) p.(=)


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