Variant #0000806696 (NC_000015.9:g.43897498G>A, NM_153700.2:c.3894C>T (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.43897498G>A
DNA change (hg38) -
Published as STRC(NM_153700.2):c.3894C>T (p.H1298=)
ISCN -
DB-ID STRC_000101
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.-87978G>A r.(?) p.(=)
STRC NM_153700.2 -?/. - c.3894C>T r.(?) p.(His1298=)
CATSPER2 NM_172095.1 -?/. - c.*25401C>T r.(=) p.(=)


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