Variant #0000944777 (NC_000011.9:g.67953336C>T, NM_017635.3:c.220G>A (SUV420H1))

Chromosome 11
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.67953336C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SUV420H1_000017 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1250854401
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-14 14:56:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUV420H1 NM_017635.3 ?/. - c.220G>A r.(?) p.(Ala74Thr)


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