Variant #0000611317 (NC_000007.13:g.92731586A>G, NM_017654.3:c.3825T>C (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.92731586A>G
DNA change (hg38) g.93102273A>G
Published as SAMD9(NM_001193307.1):c.3825T>C (p.(Phe1275=)), SAMD9(NM_017654.4):c.3825T>C (p.F1275=)
ISCN -
DB-ID SAMD9_000016 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) 0.01503 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAMD9 NM_017654.3 -?/. - c.3825T>C r.(?) p.(Phe1275=)


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