Variant #0001031843 (NC_000001.10:g.236715417A>T, NC_000001.10(NM_018072.5):c.6238-10T>A (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.236715417A>T
DNA change (hg38) -
Published as HEATR1(NM_018072.6):c.6238-10T>A
ISCN -
DB-ID HEATR1_000021
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) 0.00023 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 2025-05-05 21:14:00 +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.*3956A>T r.(=) p.(=)
HEATR1 NM_018072.5 -?/. - c.6238-10T>A r.(=) p.(=)


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