Variant #0000996720 (NC_000007.13:g.92731344T>C, NM_017654.3:c.4067A>G (SAMD9))

Chromosome 7
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.92731344T>C
DNA change (hg38) -
Published as SAMD9(NM_001193307.1):c.4067A>G (p.(Glu1356Gly)), SAMD9(NM_017654.4):c.4067A>G (p.E1356G)
ISCN -
DB-ID SAMD9_000056 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) 0.00067 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
SAMD9 NM_017654.3 -?/. - c.4067A>G r.(?) p.(Glu1356Gly)


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