Variant #0000610882 (NC_000007.13:g.141414223T>C, NC_000007.13(NM_001105558.1):c.539+18T>C (WEE2))

Chromosome 7
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.141414223T>C
DNA change (hg38) g.141714423T>C
Published as WEE2(NM_001105558.1):c.539+18T>C
ISCN -
DB-ID WEE2_000001
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WEE2 NM_001105558.1 -?/. - c.539+18T>C r.(=) p.(=)
WEE2-AS1 NR_015392.1 -?/. - n.657-49A>G r.(?) -


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