Variant #0000799199 (NC_000001.10:g.236732427G>A, NC_000001.10(NM_018072.5):c.3949-3C>T (HEATR1))

Chromosome 1
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.236732427G>A
DNA change (hg38) -
Published as HEATR1(NM_018072.5):c.3949-3C>T (p.?)
ISCN -
DB-ID HEATR1_000019
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) 0.03183 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LGALS8 NM_006499.4 -?/. - c.*20966G>A r.(=) p.(=)
HEATR1 NM_018072.5 -?/. - c.3949-3C>T r.spl? p.?


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