Variant #0001000223 (NC_000012.11:g.53722387C>A, NM_001173467.1:c.839G>T (SP7))

Chromosome 12
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.53722387C>A
DNA change (hg38) -
Published as SP7(NM_001173467.1):c.839G>T (p.(Arg280Leu)), SP7(NM_001300837.1):c.785G>T (p.R262L)
ISCN -
DB-ID SP7_000005 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) 0.00019 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     
SP7 NM_001173467.1 -?/. - c.839G>T r.(?) p.(Arg280Leu)


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