Variant #0000799545 (NC_000001.10:g.877590C>T, NM_152486.2:c.944C>T (SAMD11))

Chromosome 1
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.877590C>T
DNA change (hg38) -
Published as SAMD11(NM_152486.3):c.944C>T (p.P315L)
ISCN -
DB-ID SAMD11_000027
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.*2484G>A r.(=) p.(=)
SAMD11 NM_152486.2 ?/. - c.944C>T r.(?) p.(Pro315Leu)


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