Variant #0001035678 (NC_000006.11:g.31864040C>G, NM_000063.4:c.-31490C>G (C2))

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.31864040C>G
DNA change (hg38) -
Published as EHMT2(NM_006709.5):c.582G>C (p.(Gln194His))
ISCN -
DB-ID C2_000070
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 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     
C2 NM_000063.4 -?/. - c.-31490C>G r.(?) p.(=)
EHMT2 NM_006709.3 -?/. - c.582G>C r.(?) p.(Gln194His)
ZBTB12 NM_181842.2 -?/. - c.*3663G>C r.(=) p.(=)


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