Variant #0000726471 (NC_000017.10:g.4439699G>A, NM_014520.3:c.*3011C>T (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.4439699G>A
DNA change (hg38) -
Published as SPNS2(NM_001124758.3):c.1585G>A (p.D529N)
ISCN -
DB-ID MYBBP1A_000025
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPNS2 NM_001124758.1 ?/. - c.1585G>A r.(?) p.(Asp529Asn)
MYBBP1A NM_014520.3 ?/. - c.*3011C>T r.(=) p.(=)


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