Variant #0000253066 (NC_000015.9:g.25601030A>G, NC_000015.9(NM_000462.3):c.2133+9T>C (UBE3A))

Chromosome 15
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.25601030A>G
DNA change (hg38) g.25355883A>G
Published as UBE3A(NM_000462.5):c.2133+9T>C, UBE3A(NM_001354543.1):c.2064+9T>C, UBE3A(NM_130838.1):c.2064+9T>C
ISCN -
DB-ID UBE3A_001031 See all 3 reported entries
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) 0.00455 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3A NM_000462.3 -?/. - c.2133+9T>C r.(=) p.(=)
UBE3A NM_130839.2 -?/. - c.2124+9T>C r.(=) p.(=)


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