Variant #0000304227 (NC_000001.10:g.881627G>A, NM_152486.2:c.*2094G>A (SAMD11))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.881627G>A
DNA change (hg38) g.946247G>A
Published as NOC2L(NM_015658.4):c.1843C>T (p.L615=)
ISCN -
DB-ID NOC2L_000001
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) 0.57027 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOC2L NM_015658.3 -/. - c.1843C>T r.(?) p.(Leu615=)
SAMD11 NM_152486.2 -/. - c.*2094G>A r.(=) p.(=)


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