Variant #0000894997 (NC_000019.9:g.41029399C>A, NM_020971.2:c.3710C>A (SPTBN4))

Chromosome 19
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.41029399C>A
DNA change (hg38) -
Published as SPTBN4(NM_020971.2):c.3710C>A (p.(Ala1237Asp))
ISCN -
DB-ID SPTBN4_000031
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) 0.00525 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 2022-11-01 13:41:49 +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     
SPTBN4 NM_020971.2 -/. - c.3710C>A r.(?) p.(Ala1237Asp)


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