Variant #0000286134 (NC_000014.8:g.65544630C>T, NC_000014.8(NM_002382.4):c.295+1G>A (MAX))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65544630C>T
DNA change (hg38) g.65077912C>T
Published as MAX(NM_145113.3):c.295+1G>A
ISCN -
DB-ID MAX_000002 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHURC1-FNTB NM_001202558.1 +/. - c.*16600C>T r.(=) p.(=)
FNTB NM_002028.3 +/. - c.*16600C>T r.(=) p.(=)
MAX NM_002382.4 +/. - c.295+1G>A r.spl? p.?


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