Variant #0000533073 (NC_000007.13:g.92763782T>C, NM_152703.2:c.1503A>G (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.92763782T>C
DNA change (hg38) g.93134469T>C
Published as SAMD9L(NM_152703.4):c.1503A>G (p.R501=), SAMD9L(NM_152703.5):c.1503A>G (p.(Arg501=), p.R501=)
ISCN -
DB-ID SAMD9L_000008 See all 3 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) 0.00224 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.1503A>G r.(?) p.(Arg501=)


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