Variant #0000693674 (NC_000023.10:g.54957221C>T, NM_002625.2:c.*2615G>A (PFKFB1))

Chromosome X
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.54957221C>T
DNA change (hg38) -
Published as TRO(NM_001039705.2):c.4064C>T (p.(Thr1355Met))
ISCN -
DB-ID TRO_000044
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) 1.0E-5 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKFB1 NM_002625.2 ?/. - c.*2615G>A r.(=) p.(=)
TRO NM_016157.2 ?/. - c.1987-416C>T r.(=) p.(=)


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