Variant #0000994685 (NC_000005.9:g.138730647C>T, NM_001161546.1:c.124G>A (PROB1))

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.138730647C>T
DNA change (hg38) -
Published as PROB1(NM_001161546.1):c.124G>A (p.(Glu42Lys))
ISCN -
DB-ID PROB1_000002
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PROB1 NM_001161546.1 -?/. - c.124G>A r.(?) p.(Glu42Lys)
SPATA24 NM_194296.1 -?/. - c.*1842G>A r.(=) p.(=)


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