Variant #0000577289 (NC_000023.10:g.70523328C>T, NM_007363.4:c.*3402C>T (NONO))

Chromosome X
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.70523328C>T
DNA change (hg38) g.71303478C>T
Published as ITGB1BP2(NM_012278.3):c.430C>T (p.R144W)
ISCN -
DB-ID ITGB1BP2_000006
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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
NONO NM_007363.4 -?/. - c.*3402C>T r.(=) p.(=)
ITGB1BP2 NM_012278.1 -?/. - c.430C>T r.(?) p.(Arg144Trp)


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