Variant #0000562065 (NC_000017.10:g.4446383C>T, NM_014520.3:c.2717G>A (MYBBP1A))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4446383C>T
DNA change (hg38) g.4543088C>T
Published as MYBBP1A(NM_014520.3):c.2717G>A (p.R906Q)
ISCN -
DB-ID MYBBP1A_000014
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) 0.00037 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*5640C>T r.(=) p.(=)
MYBBP1A NM_014520.3 -?/. - c.2717G>A r.(?) p.(Arg906Gln)


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