Variant #0000688154 (NC_000001.10:g.36564371C>T, NM_017825.2:c.*5384C>T (ADPRHL2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36564371C>T
DNA change (hg38) -
Published as COL8A2(NM_005202.3):c.911G>A (p.R304Q)
ISCN -
DB-ID ADPRHL2_000021
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) 0.00011 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
COL8A2 NM_005202.2 ?/. - c.911G>A r.(?) p.(Arg304Gln)
ADPRHL2 NM_017825.2 ?/. - c.*5384C>T r.(=) p.(=)


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