Variant #0000502973 (NC_000001.10:g.145330796A>T, NM_001039703.4:c.4676A>T (NBPF10))

Chromosome 1
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.145330796A>T
DNA change (hg38) g.146107403T>A
Published as NBPF10(NM_001039703.4):c.4901A>T (p.(Tyr1634Phe))
ISCN -
DB-ID NBPF10_000013
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) 0.0001 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NBPF10 NM_001039703.4 -?/. - c.4676A>T r.(?) p.(Tyr1559Phe)


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