Variant #0000995326 (NC_000006.11:g.126072990A>T, NM_012259.2:c.127A>T (HEY2))

Chromosome 6
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.126072990A>T
DNA change (hg38) -
Published as HEY2(NM_012259.2):c.127A>T (p.(Thr43Ser)), HEY2(NM_012259.3):c.127A>T (p.T43S)
ISCN -
DB-ID HEY2_000026 See all 2 reported entries
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) 0.00097 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +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     
HEY2 NM_012259.2 -?/. - c.127A>T r.(?) p.(Thr43Ser)


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