Variant #0000311796 (NC_000007.13:g.100225847C>T, NM_003227.3:c.1473G>A (TFR2))

Chromosome 7
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.100225847C>T
DNA change (hg38) g.100628224C>T
Published as TFR2(NM_003227.3):c.1473G>A (p.E491=), TFR2(NM_003227.4):c.1473G>A (p.(Glu491=), p.E491=)
ISCN -
DB-ID TFR2_000040 See all 8 reported entries
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) 0.00316 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFR2 NM_003227.3 ?/. - c.1473G>A r.(?) p.(Glu491=)


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