Variant #0000892057 (NC_000015.9:g.43910286C>A, NM_153700.2:c.333G>T (STRC))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43910286C>A
DNA change (hg38) -
Published as STRC(NM_153700.2):c.333G>T (p.G111=)
ISCN -
DB-ID STRC_000087 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.-75190C>A r.(?) p.(=)
STRC NM_153700.2 -/. - c.333G>T r.(?) p.(Gly111=)
CATSPER2 NM_172095.1 -/. - c.*12613G>T r.(=) p.(=)


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