Variant #0001026397 (NC_000014.8:g.65527977C>T, NM_002382.4:c.*15217G>A (MAX))

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.65527977C>T
DNA change (hg38) -
Published as CHURC1-FNTB(NM_001202559.1):c.1444C>T (p.P482S), FNTB(NM_002028.4):c.1261C>T (p.P421S)
ISCN -
DB-ID CHURC1_000005
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) 6.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
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.1123C>T r.(?) p.(Pro375Ser)
FNTB NM_002028.3 ?/. - c.1261C>T r.(?) p.(Pro421Ser)
GPX2 NM_002083.3 ?/. - c.-118533G>A r.(?) p.(=)
MAX NM_002382.4 ?/. - c.*15217G>A r.(=) p.(=)
CHURC1 NM_145165.3 ?/. - c.*129029C>T r.(=) p.(=)
RAB15 NM_198686.2 ?/. - c.-89183G>A r.(?) p.(=)


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