Variant #0000681477 (NC_000019.9:g.50027953C>G, NM_001136019.2:c.791C>G (FCGRT))

Chromosome 19
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.50027953C>G
DNA change (hg38) -
Published as FCGRT(NM_001136019.3):c.791C>G (p.T264R)
ISCN -
DB-ID FCGRT_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +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     
FCGRT NM_001136019.2 -?/. - c.791C>G r.(?) p.(Thr264Arg)
RCN3 NM_020650.2 -?/. - c.-3369C>G r.(?) p.(=)


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