Variant #0001000062 (NC_000012.11:g.48545060G>A, NM_000289.5:c.*5569G>A (PFKM))

Chromosome 12
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.48545060G>A
DNA change (hg38) -
Published as ASB8(NM_024095.3):c.158C>T (p.(Thr53Ile))
ISCN -
DB-ID ASB8_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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKM NM_000289.5 ?/. - c.*5569G>A r.(=) p.(=)
PFKM NM_001166686.1 ?/. - c.*5569G>A r.(=) p.(=)
SENP1 NM_001267594.1 ?/. - c.-45294C>T r.(?) p.(=)
ASB8 NM_024095.3 ?/. - c.158C>T r.(?) p.(Thr53Ile)


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