Variant #0001039727 (NC_000013.10:g.51961524G>T, NM_012141.2:c.892C>A (INTS6))

Chromosome 13
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.51961524G>T
DNA change (hg38) -
Published as INTS6(NM_012141.3):c.892C>A (p.(Leu298Ile))
ISCN -
DB-ID INTS6_000002
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 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINE3 NM_001101320.1 ?/. - c.*25391G>T r.(=) p.(=)
INTS6 NM_012141.2 ?/. - c.892C>A r.(?) p.(Leu298Ile)


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