Variant #0000806465 (NC_000014.8:g.65544614C>T, NC_000014.8(NM_002382.4):c.295+17G>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.65544614C>T
DNA change (hg38) -
Published as MAX(NM_145113.3):c.295+17G>A
ISCN -
DB-ID CHURC1-FNTB_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) 0 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2021-09-17 14:40:49 +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.*16584C>T r.(=) p.(=)
FNTB NM_002028.3 -?/. - c.*16584C>T r.(=) p.(=)
MAX NM_002382.4 -?/. - c.295+17G>A r.(=) p.(=)


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