Variant #0000576766 (NC_000023.10:g.54956384G>A, NM_002625.2:c.*3452C>T (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.54956384G>A
DNA change (hg38) g.54929951G>A
Published as TRO(NM_001039705.2):c.3227G>A (p.S1076N)
ISCN -
DB-ID TRO_000038
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.*3452C>T r.(=) p.(=)
TRO NM_016157.2 ?/. - c.1986+1241G>A r.(=) p.(=)


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