Variant #0000883623 (NC_000001.10:g.874840_874888del, NC_000001.10(NM_152486.2):c.706_706+48del (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.874840_874888del
DNA change (hg38) -
Published as SAMD11(NM_152486.4):c.683_706+25del
ISCN -
DB-ID SAMD11_000041
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +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.*5209_*5257del r.(=) p.(=)
SAMD11 NM_152486.2 -?/. - c.706_706+48del r.spl? p.?


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