Variant #0000623065 (NC_000013.10:g.41639443_41639446dup, NC_000013.10(NM_007187.3):c.262+20_262+23dup (WBP4))

Chromosome 13
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.41639443_41639446dup
DNA change (hg38) g.41065307_41065310dup
Published as WBP4(NM_007187.5):c.262+21_262+24dupAAAA
ISCN -
DB-ID ELF1_000005
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-06 12:43:26 +01:00 (CET)
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     
WBP4 NM_007187.3 -?/. - c.262+20_262+23dup r.(=) p.(=)
ELF1 NM_172373.3 -?/. - c.-46294_-46291dup r.(?) p.(=)


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