Variant #0000554337 (NC_000015.9:g.43910201G>T, NM_153700.2:c.418C>A (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.43910201G>T
DNA change (hg38) g.43618003G>T
Published as STRC(NM_153700.2):c.418C>A (p.L140I)
ISCN -
DB-ID STRC_000085
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) 2.0E-5 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 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.-75275G>T r.(?) p.(=)
STRC NM_153700.2 ?/. - c.418C>A r.(?) p.(Leu140Ile)
CATSPER2 NM_172095.1 ?/. - c.*12698C>A r.(=) p.(=)


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