Variant #0000554329 (NC_000015.9:g.43903187dup, NC_000015.9(NM_153700.2):c.3307-5dup (STRC))

Chromosome 15
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.43903187dup
DNA change (hg38) g.43610989dup
Published as STRC(NM_153700.2):c.3307-5dupT
ISCN -
DB-ID STRC_000077
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_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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CKMT1A NM_001015001.1 -?/. - c.-82289dup r.(?) p.(=)
STRC NM_153700.2 -?/. - c.3307-5dup r.spl? p.?
CATSPER2 NM_172095.1 -?/. - c.*19712dup r.(?) p.(=)


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