Variant #0000717720 (NC_000001.10:g.878029C>T, NM_152486.2:c.1155C>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.878029C>T
DNA change (hg38) -
Published as SAMD11(NM_152486.3):c.1155C>T (p.N385=), SAMD11(NM_152486.4):c.1155C>T (p.N385=)
ISCN -
DB-ID SAMD11_000021 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) 0.00191 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*2045G>A r.(=) p.(=)
SAMD11 NM_152486.2 -?/. - c.1155C>T r.(?) p.(Asn385=)


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