Variant #0000576768 (NC_000023.10:g.54957045T>G, NM_002625.2:c.*2791A>C (PFKFB1))

Chromosome X
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.54957045T>G
DNA change (hg38) g.54930612T>G
Published as TRO(NM_001039705.2):c.3888T>G (p.(Asn1296Lys))
ISCN -
DB-ID TRO_000040
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) 0.00019 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKFB1 NM_002625.2 -?/. - c.*2791A>C r.(=) p.(=)
TRO NM_016157.2 -?/. - c.1987-592T>G r.(=) p.(=)


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