Variant #0000978977 (NC_000010.10:g.14941289A>T, NC_000010.10(NM_024670.3):c.670-249A>T (SUV39H2))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.14941289A>T
DNA change (hg38) -
Published as DCLRE1C(NM_001350965.2):c.1805T>A (p.(Leu602Gln))
ISCN -
DB-ID SUV39H2_000008
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 2024-04-19 20:27:30 +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     
SUV39H2 NM_024670.3 ?/. - c.670-249A>T r.(=) p.(=)


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