Variant #0000614554 (NC_000013.10:g.28008323G>A, NM_002097.2:c.610G>A (GTF3A))

Chromosome 13
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.28008323G>A
DNA change (hg38) g.27434186G>A
Published as GTF3A(NM_002097.3):c.610G>A (p.E204K)
ISCN -
DB-ID GTF3A_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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
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     
GTF3A NM_002097.2 ?/. - c.610G>A r.(?) p.(Glu204Lys)
MTIF3 NM_152912.4 ?/. - c.*1489C>T r.(=) p.(=)


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