Variant #0000654121 (NC_000001.10:g.877978G>A, NM_152486.2:c.1104G>A (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.877978G>A
DNA change (hg38) g.942598G>A
Published as SAMD11(NM_001385640.1):c.1596G>A (p.L532=), SAMD11(NM_152486.3):c.1104G>A (p.L368=)
ISCN -
DB-ID SAMD11_000013 See all 2 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) 0.00047 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOC2L NM_015658.3 -?/. - c.*2096C>T r.(=) p.(=)
SAMD11 NM_152486.2 -?/. - c.1104G>A r.(?) p.(Leu368=)


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