Variant #0001040360 (NC_000015.9:g.43906252C>G, NC_000015.9(NM_153700.2):c.2314-1G>C (STRC))

Chromosome 15
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.43906252C>G
DNA change (hg38) -
Published as STRC(NM_153700.2):c.2314-1G>C
ISCN -
DB-ID STRC_000106 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) 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 2025-05-05 21:14:00 +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     
CKMT1A NM_001015001.1 ?/. - c.-79224C>G r.(?) p.(=)
STRC NM_153700.2 ?/. - c.2314-1G>C r.spl? p.?
CATSPER2 NM_172095.1 ?/. - c.*16647G>C r.(=) p.(=)


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