Variant #0000549899 (NC_000013.10:g.115086580T>C, NC_000013.10(NM_032436.2):c.-178-5T>C (CHAMP1))

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.115086580T>C
DNA change (hg38) g.114321105T>C
Published as CHAMP1(NM_001164144.1):c.-175-5T>C (p.(=))
ISCN -
DB-ID CHAMP1_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-04 15:08:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHAMP1 NM_032436.2 -?/. - c.-178-5T>C r.spl? p.?


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