Variant #0000568600 (NC_000019.9:g.5844667T>G, NM_000150.2:c.-6120A>C (FUT6))

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.5844667T>G
DNA change (hg38) g.5844656T>G
Published as FUT3(NM_000149.3):c.184A>C (p.(Thr62Pro))
ISCN -
DB-ID FUT3_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUT3 NM_000149.3 -?/. - c.184A>C r.(?) p.(Thr62Pro)
FUT6 NM_000150.2 -?/. - c.-6120A>C r.(?) p.(=)


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