Variant #0000678803 (NC_000010.10:g.127512283A>G, NM_000375.2:c.-712T>C (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.127512283A>G
DNA change (hg38) -
Published as BCCIP(NM_078469.2):c.157A>G (p.I53V)
ISCN -
DB-ID BCCIP_000004
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) 5.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UROS NM_000375.2 -?/. - c.-712T>C r.(?) p.(=)
BCCIP NM_016567.3 -?/. - c.157A>G r.(?) p.(Ile53Val)
DHX32 NM_018180.2 -?/. - c.*12973T>C r.(=) p.(=)


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