Variant #0000981221 (NC_000015.9:g.43932701A>G, NM_153700.2:c.-21781T>C (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.43932701A>G
DNA change (hg38) -
Published as CATSPER2(NM_172095.4):c.389-7T>C
ISCN -
DB-ID CKMT1A_000002
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) 0.00083 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.-52775A>G r.(?) p.(=)
STRC NM_153700.2 -?/. - c.-21781T>C r.(?) p.(=)
CATSPER2 NM_172095.1 -?/. - c.389-7T>C r.(=) p.(=)


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