Variant #0000689934 (NC_000007.13:g.143175136C>G, NC_000007.13(NR_033897.1):n.207-26731C>G (EPHA1-AS1))

Chromosome 7
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.143175136C>G
DNA change (hg38) -
Published as TAS2R41(NM_176883.2):c.171C>G (p.C57W)
ISCN -
DB-ID EPHA1-AS1_000001
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_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     
TAS2R41 NM_176883.2 ?/. - c.171C>G r.(?) p.(Cys57Trp)
EPHA1-AS1 NR_033897.1 ?/. - n.207-26731C>G r.(?) -


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