Variant #0000887512 (NC_000007.13:g.100243937C>T, NM_003227.3:c.-4805G>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.100243937C>T
DNA change (hg38) -
Published as ACTL6B(NM_016188.5):c.1135G>A (p.A379T)
ISCN -
DB-ID ACTL6B_000015
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFR2 NM_003227.3 ?/. - c.-4805G>A r.(?) p.(=)
ACTL6B NM_016188.4 ?/. - c.1135G>A r.(?) p.(Ala379Thr)


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