Variant #0000326082 (NC_000019.9:g.5831634G>T, NM_000150.2:c.945C>A (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.5831634G>T
DNA change (hg38) g.5831623G>T
Published as FUT6(NM_000150.2):c.945C>A (p.(Tyr315Ter))
ISCN -
DB-ID FUT6_000001
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) 0.01715 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 10:31:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUT6 NM_000150.2 -?/. - c.945C>A r.(?) p.(Tyr315Ter)
NRTN NM_004558.3 -?/. - c.*3450G>T r.(=) p.(=)


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