Variant #0001026396 (NC_000014.8:g.65507574C>T, NM_002382.4:c.*35620G>A (MAX))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65507574C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CHURC1_000004
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) 7.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.621C>T r.(?) p.(=)
FNTB NM_002028.3 -?/. - c.759C>T r.(?) p.(=)
GPX2 NM_002083.3 -?/. - c.-98130G>A r.(?) p.(=)
MAX NM_002382.4 -?/. - c.*35620G>A r.(=) p.(=)
CHURC1 NM_145165.3 -?/. - c.*108626C>T r.(=) p.(=)
RAB15 NM_198686.2 -?/. - c.-68780G>A r.(?) p.(=)


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