Variant #0000977842 (NC_000007.13:g.73944180A>G, NM_016328.2:c.1207A>G (GTF2IRD1))

Chromosome 7
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.73944180A>G
DNA change (hg38) -
Published as GTF2IRD1(NM_005685.4):c.1207A>G (p.(Thr403Ala))
ISCN -
DB-ID GTF2IRD1_000006
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 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTF2IRD1 NM_016328.2 -?/. - c.1207A>G r.(?) p.(Thr403Ala)


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