Variant #0000275559 (NC_000011.9:g.117299424C>T, NM_020693.2:c.5962G>A (DSCAML1))

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.117299424C>T
DNA change (hg38) g.117428708C>T
Published as DSCAML1(NM_020693.2):c.5962G>A (p.(Ala1988Thr)), DSCAML1(NM_020693.3):c.5962G>A (p.A1988T)
ISCN -
DB-ID DSCAML1_000002 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) 0.00072 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSCAML1 NM_020693.2 ?/. - c.5962G>A r.(?) p.(Ala1988Thr)


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