Variant #0000560707 (NC_000017.10:g.26686416G>A, NM_001080837.2:c.*4874C>T (SEBOX))

Chromosome 17
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.26686416G>A
DNA change (hg38) g.28359393G>A
Published as TMEM199(NM_152464.1):c.364G>A (p.(Val122Ile))
ISCN -
DB-ID POLDIP2_000002
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) 0.04591 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEBOX NM_001080837.2 -?/. - c.*4874C>T r.(=) p.(=)
POLDIP2 NM_015584.3 -?/. - c.-1943C>T r.(?) p.(=)
TNFAIP1 NM_021137.4 -?/. - c.*14790G>A r.(=) p.(=)
TMEM199 NM_152464.1 -?/. - c.364G>A r.(?) p.(Val122Ile)


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