Variant #0000554338 (NC_000015.9:g.43910210G>C, NM_153700.2:c.409C>G (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.43910210G>C
DNA change (hg38) g.43618012G>C
Published as STRC(NM_153700.2):c.409C>G (p.L137V)
ISCN -
DB-ID STRC_000086
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 2019-07-18 18:22:55 +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.-75266G>C r.(?) p.(=)
STRC NM_153700.2 -?/. - c.409C>G r.(?) p.(Leu137Val)
CATSPER2 NM_172095.1 -?/. - c.*12689C>G r.(=) p.(=)


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