Variant #0000518866 (NC_000003.11:g.195794391A>G, NM_001128148.1:c.1038T>C (TFRC))

Chromosome 3
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.195794391A>G
DNA change (hg38) g.196067520A>G
Published as TFRC(NM_003234.3):c.1038T>C (p.F346=), TFRC(NM_003234.4):c.1038T>C (p.F346=)
ISCN -
DB-ID TFRC_000006 See all 2 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) 0.00025 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
TFRC NM_001128148.1 -?/. - c.1038T>C r.(?) p.(Phe346=)


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