Variant #0000998758 (NC_000011.9:g.117691589C>T, NM_021603.3:c.155G>A (FXYD2))

Chromosome 11
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.117691589C>T
DNA change (hg38) -
Published as FXYD2(NM_001680.4):c.161G>A (p.(Gly54Asp))
ISCN -
DB-ID FXYD2_000015
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) 4.0E-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 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     
FXYD6-FXYD2 NM_001204268.1 ?/. - c.395G>A r.(?) p.(Gly132Asp)
FXYD2 NM_021603.3 ?/. - c.155G>A r.(?) p.(Gly52Asp)
FXYD6 NM_022003.3 ?/. - c.*17425G>A r.(=) p.(=)


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