Variant #0001046738 (NC_000019.9:g.41018736_41018744dup, NM_020971.2:c.2040_2048dup (SPTBN4))

Chromosome 19
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.41018736_41018744dup
DNA change (hg38) -
Published as SPTBN4(NM_020971.3):c.2040_2048dupCGCAGCGGG (p.A681_G683dup)
ISCN -
DB-ID SPTBN4_000050
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-07-08 13:22:38 +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     
SPTBN4 NM_020971.2 -?/. - c.2040_2048dup r.(?) p.(Ala681_Gly683dup)


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