Variant #0000996739 (NC_000007.13:g.92761147dup, NM_152703.2:c.4140dup (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.92761147dup
DNA change (hg38) -
Published as SAMD9L(NM_152703.2):c.4140dupA (p.(Gln1381fs)), SAMD9L(NM_152703.4):c.4140dupA (p.Q1381Tfs*77), SAMD9L(NM_152703.5):c.4140dupA (p.Q1381Tfs*77)
ISCN -
DB-ID SAMD9L_000010 See all 4 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) 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAMD9L NM_152703.2 ?/. - c.4140dup r.(?) p.(Gln1381ThrfsTer77)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.