Variant #0001001095 (NC_000014.8:g.65264430_65264450del, NC_000014.8(NM_000347.5):c.1179_1182+17del (SPTB))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65264430_65264450del
DNA change (hg38) -
Published as SPTB(NM_001024858.2):c.1179_1182+17delCAGGGTACCACAGCATTTTCC (p.(Asn393fs))
ISCN -
DB-ID SPTB_000183
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 2024-08-28 13:16:32 +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     
SPTB NM_000347.5 +?/. - c.1179_1182+17del r.(?) p.(Leu388_Arg394del)
SPTB NM_001024858.2 +?/. - c.1179_1182+17del r.(?) p.(Leu388_Arg394del)


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