Variant #0001001098 (NC_000014.8:g.65406308G>T, NC_000014.8(NM_001202558.1):c.6+15464G>T (CHURC1-FNTB))

Chromosome 14
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.65406308G>T
DNA change (hg38) -
Published as GPX2(NM_002083.3):c.471C>A (p.(Phe157Leu))
ISCN -
DB-ID CHURC1_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     
CHURC1-FNTB NM_001202558.1 ?/. - c.6+15464G>T r.(=) p.(=)
FNTB NM_002028.3 ?/. - c.-47364G>T r.(?) p.(=)
GPX2 NM_002083.3 ?/. - c.471C>A r.(?) p.?
CHURC1 NM_145165.3 ?/. - c.*7360G>T r.(=) p.(=)
RAB15 NM_198686.2 ?/. - c.*8907C>A r.(=) p.(=)


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