Variant #0000524382 (NC_000005.9:g.138728256G>A, NM_016459.3:c.-2711C>T (MZB1))

Chromosome 5
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.138728256G>A
DNA change (hg38) g.139392567G>A
Published as PROB1(NM_001161546.1):c.2515C>T (p.(Pro839Ser))
ISCN -
DB-ID MZB1_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) 0.00439 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 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     
PROB1 NM_001161546.1 -?/. - c.2515C>T r.(?) p.(Pro839Ser)
MZB1 NM_016459.3 -?/. - c.-2711C>T r.(?) p.(=)
SPATA24 NM_194296.1 -?/. - c.*4233C>T r.(=) p.(=)


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