Variant #0000259166 (NC_000017.10:g.79974731T>C, NM_024083.2:c.1461T>C (ASPSCR1))

Chromosome 17
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.79974731T>C
DNA change (hg38) g.82016855T>C
Published as ASPSCR1(NM_001251888.2):c.1743T>C (p.D581=)
ISCN -
DB-ID ASPSCR1_000001
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) 0.58287 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPSCR1 NM_024083.2 -/. - c.1461T>C r.(?) p.(Asp487=)
STRA13 NM_144998.3 -/. - c.*2350A>G r.(=) p.(=)


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