Variant #0000678802 (NC_000010.10:g.127512219A>T, NM_000375.2:c.-648T>A (UROS))

Chromosome 10
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.127512219A>T
DNA change (hg38) -
Published as BCCIP(NM_078469.2):c.93A>T (p.E31D)
ISCN -
DB-ID BCCIP_000003
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UROS NM_000375.2 -?/. - c.-648T>A r.(?) p.(=)
BCCIP NM_016567.3 -?/. - c.93A>T r.(?) p.(Glu31Asp)
DHX32 NM_018180.2 -?/. - c.*13037T>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.