Variant #0000058487 (NC_000004.11:g.109971414T>A, NC_000004.11(NM_198721.2):c.368-79A>T (COL25A1))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.109971414T>A
DNA change (hg38) g.109050258T>A
Published as -
ISCN -
DB-ID COL25A1_000007
Variant remarks -
Reference PubMed: Shinwari 2015, Journal: Shinwari 2015
ClinVar ID -
dbSNP ID rs1863292
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-02-14 19:25:50 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL25A1 NM_198721.2 -/. 3i c.368-79A>T r.(=) p.(=)


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