Variant #0001055200 (NC_000015.9:g.74473250C>A, NM_001142617.1:c.1713G>T (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.74473250C>A
DNA change (hg38) -
Published as STRA6(NM_001199042.1):c.1830G>T (p.K610N), STRA6(NM_022369.4):c.1713G>T (p.(Lys571Asn))
ISCN -
DB-ID STRA6_000001 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) 9.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRA6 NM_001142617.1 ?/. - c.1713G>T r.(?) p.(Lys571Asn)
ISLR NM_005545.3 ?/. - c.*4764C>A r.(=) p.(=)


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