Variant #0000615316 (NC_000015.9:g.43908298C>G, NM_153700.2:c.1466G>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.43908298C>G
DNA change (hg38) g.43616100C>G
Published as -
ISCN -
DB-ID STRC_000093
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CKMT1A NM_001015001.1 ?/. - c.-77178C>G r.(?) p.(=)
STRC NM_153700.2 ?/. - c.1466G>C r.(?) p.(Ser489Thr)
CATSPER2 NM_172095.1 ?/. - c.*14601G>C r.(=) p.(=)


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