Variant #0000311799 (NC_000007.13:g.100238335C>T, NM_003227.3:c.447G>A (TFR2))

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.100238335C>T
DNA change (hg38) g.100640712C>T
Published as TFR2(NM_003227.4):c.447G>A (p.G149=)
ISCN -
DB-ID TFR2_000063
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) 0.00066 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 2021-09-17 14:40:49 +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.447G>A r.(?) p.(Gly149=)
ACTL6B NM_016188.4 -?/. - c.*2534G>A r.(=) p.(=)


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