Variant #0000324593 (NC_000016.9:g.10864155C>T, NM_002484.2:c.*1193C>T (NUBP1))

Chromosome 16
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.10864155C>T
DNA change (hg38) g.10770298C>T
Published as TVP23A(NM_001079512.2):c.616G>A (p.(Glu206Lys))
ISCN -
DB-ID TVP23A_000001
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) 0.00013 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TVP23A NM_001079512.2 -?/. - c.616G>A r.(?) p.(Glu206Lys)
NUBP1 NM_002484.2 -?/. - c.*1193C>T r.(=) p.(=)


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