Variant #0001014391 (NC_000007.13:g.92764419A>G, NM_152703.2:c.866T>C (SAMD9L))

Chromosome 7
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.92764419A>G
DNA change (hg38) -
Published as SAMD9L(NM_001303496.1):c.866T>C (p.(Phe289Ser)), SAMD9L(NM_152703.5):c.866T>C (p.F289S)
ISCN -
DB-ID SAMD9L_000015 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) 0.01804 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAMD9L NM_152703.2 -/. - c.866T>C r.(?) p.(Phe289Ser)


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