Variant #0000506129 (NC_000001.10:g.236758926T>C, NM_018072.5:c.1004A>G (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.236758926T>C
DNA change (hg38) g.236595626T>C
Published as HEATR1(NM_018072.5):c.1004A>G (p.(His335Arg))
ISCN -
DB-ID HEATR1_000015
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) 0.00031 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LGALS8 NM_006499.4 -?/. - c.*47465T>C r.(=) p.(=)
HEATR1 NM_018072.5 -?/. - c.1004A>G r.(?) p.(His335Arg)


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