Variant #0000321384 (NC_000001.10:g.236714309_236714310del, NC_000001.10(NM_018072.5):c.6347-4_6347-3del (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.236714309_236714310del
DNA change (hg38) g.236551009_236551010del
Published as HEATR1(NM_018072.5):c.6347-4_6347-3del (p.?)
ISCN -
DB-ID HEATR1_000002
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 2018-01-15 20:58:59 +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     
LGALS8 NM_006499.4 -?/. - c.*2848_*2849del r.(=) p.(=)
HEATR1 NM_018072.5 -?/. - c.6347-4_6347-3del r.spl? p.?


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