Variant #0000563730 (NC_000017.10:g.79974915_79974916del, NM_024083.2:c.1574_1575del (ASPSCR1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.79974915_79974916del
DNA change (hg38) g.82017039_82017040del
Published as ASPSCR1(NM_001251888.1):c.1856_1857delCT (p.P619Rfs*51)
ISCN -
DB-ID STRA13_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) 0.00123 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPSCR1 NM_024083.2 ?/. - c.1574_1575del r.(?) p.(Pro525ArgfsTer51)
STRA13 NM_144998.3 ?/. - c.*2165_*2166del r.(=) p.(=)


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