Variant #0000803291 (NC_000007.13:g.92761203A>G, NM_152703.2:c.4082T>C (SAMD9L))

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.92761203A>G
DNA change (hg38) -
Published as SAMD9L(NM_152703.2):c.4082T>C (p.(Val1361Ala)), SAMD9L(NM_152703.4):c.4082T>C (p.V1361A)
ISCN -
DB-ID SAMD9L_000028 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) 0.00012 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAMD9L NM_152703.2 -?/. - c.4082T>C r.(?) p.(Val1361Ala)


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