Variant #0000961177 (NC_000001.10:g.879381C>T, NM_152486.2:c.1894C>T (SAMD11))

Chromosome 1
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.879381C>T
DNA change (hg38) -
Published as SAMD11(NM_001385640.1):c.2386C>T (p.L796F)
ISCN -
DB-ID SAMD11_000060
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) 0.00125 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOC2L NM_015658.3 -?/. - c.*693G>A r.(=) p.(=)
SAMD11 NM_152486.2 -?/. - c.1894C>T r.(?) p.(Leu632Phe)


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