Variant #0000530043 (NC_000007.13:g.100245102G>A, NM_003227.3:c.-5970C>T (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.100245102G>A
DNA change (hg38) g.100647479G>A
Published as -
ISCN -
DB-ID ACTL6B_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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 11:06:33 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFR2 NM_003227.3 ?/. - c.-5970C>T r.(?) p.(=)
ACTL6B NM_016188.4 ?/. - c.724C>T r.(?) p.(Gln242Ter)


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