Variant #0000799546 (NC_000001.10:g.877627C>T, NM_152486.2:c.981C>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.877627C>T
DNA change (hg38) -
Published as SAMD11(NM_152486.3):c.981C>T (p.T327=)
ISCN -
DB-ID SAMD11_000028
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOC2L NM_015658.3 -?/. - c.*2447G>A r.(=) p.(=)
SAMD11 NM_152486.2 -?/. - c.981C>T r.(?) p.(Thr327=)


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