Variant #0000925966 (NC_000015.9:g.43908762C>T, NM_153700.2:c.1002G>A (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.43908762C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID STRC_000114
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 2023-04-16 21:50:28 +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.-76714C>T r.(?) p.(=)
STRC NM_153700.2 -?/. - c.1002G>A r.(?) p.(Pro334=)
CATSPER2 NM_172095.1 -?/. - c.*14137G>A r.(=) p.(=)


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