Variant #0000325520 (NC_000017.10:g.56598121G>A, NM_001201457.1:c.*36251C>T (TEX14))

Chromosome 17
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.56598121G>A
DNA change (hg38) g.58520760G>A
Published as SEPT4(NM_001198713.1):c.1336C>T (p.(Arg446Ter))
ISCN -
DB-ID SEPT4_000001
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) 2.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEPT4 NM_001198713.1 ?/. - c.1336C>T r.(?) p.(Arg446Ter)
TEX14 NM_001201457.1 ?/. - c.*36251C>T r.(=) p.(=)
MTMR4 NM_004687.4 ?/. - c.-2980C>T r.(?) p.(=)


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