Variant #0000329803 (NC_000004.11:g.1720002T>G, NM_006342.2:c.-3370T>G (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.1720002T>G
DNA change (hg38) g.1718275T>G
Published as TMEM129(NM_001127266.1):c.557A>C (p.(Asp186Ala))
ISCN -
DB-ID TMEM129_000003
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 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     
TACC3 NM_006342.2 -?/. - c.-3370T>G r.(?) p.(=)
TMEM129 NM_138385.3 -?/. - c.557A>C r.(?) p.(Asp186Ala)


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