Variant #0000324200 (NC_000015.9:g.74488388C>G, NM_001142617.1:c.367G>C (STRA6))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74488388C>G
DNA change (hg38) g.74196047C>G
Published as STRA6(NM_001142617.1):c.367G>C (p.(Ala123Pro)), STRA6(NM_022369.4):c.367G>C (p.A123P)
ISCN -
DB-ID STRA6_000016 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) 0.00192 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRA6 NM_001142617.1 ?/. - c.367G>C r.(?) p.(Ala123Pro)


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