Variant #0001020343 (NC_000014.8:g.65544706T>C, NM_002382.4:c.220A>G (MAX))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.65544706T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID CHURC1-FNTB_000001 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Richarda de Voer
Database submission license No license selected
Created by Richarda de Voer
Date created 2025-01-10 19:19:09 +01:00 (CET)
Date last edited 2025-01-13 16:42:41 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAX NM_002382.4 ?/. - c.220A>G r.(?) p.(Met74Val)


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