Variant #0001015168 (NC_000014.8:g.75356090dup, NC_000014.8(NM_001933.4):c.274+38dup (DLST))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.75356090dup
DNA change (hg38) -
Published as DLST(NM_001244883.1):c.274+20_274+21insT (p.(=)), DLST(NM_001933.5):c.274+38dupT
ISCN -
DB-ID DLST_000004 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-10-29 21:08:56 +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     
DLST NM_001933.4 -/. - c.274+38dup r.(=) p.(=)


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