Variant #0000912823 (NC_000007.13:g.92762433_92762436dup, NM_152703.2:c.2849_2852dup (SAMD9L))

Chromosome 7
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.92762433_92762436dup
DNA change (hg38) -
Published as SAMD9L(NM_152703.5):c.2849_2852dupACAC (p.S952Hfs*2)
ISCN -
DB-ID SAMD9L_000046
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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     
SAMD9L NM_152703.2 ?/. - c.2849_2852dup r.(?) p.(Ser952Hisfs*2)


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