Variant #0000552502 (NC_000014.8:g.31542106T>G, NM_014574.3:c.-46715A>C (STRN3))

Chromosome 14
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.31542106T>G
DNA change (hg38) g.31072900T>G
Published as AP4S1(NM_001128126.2):c.226-5T>G (p.?)
ISCN -
DB-ID AP4S1_000015
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-05 14:01:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4S1 NM_001128126.2 -?/. - c.226-5T>G r.spl? p.?
STRN3 NM_014574.3 -?/. - c.-46715A>C r.(?) p.(=)


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