Variant #0000522032 (NC_000004.11:g.1719150C>T, NM_006342.2:c.-4222C>T (TACC3))

Chromosome 4
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.1719150C>T
DNA change (hg38) g.1717423C>T
Published as TMEM129(NM_001127266.1):c.846G>A (p.(=))
ISCN -
DB-ID SLBP_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) 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
TACC3 NM_006342.2 -?/. - c.-4222C>T r.(?) p.(=)
SLBP NM_006527.2 -?/. - c.-5235G>A r.(?) p.(=)
TMEM129 NM_138385.3 -?/. - c.686G>A r.(?) p.(Trp229Ter)


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