Variant #0000721189 (NC_000007.13:g.1132178T>C, NC_000007.13(NM_032350.5):c.129+34715A>G (C7orf50))

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.1132178T>C
DNA change (hg38) -
Published as GPER1(NM_001039966.1):c.814T>C (p.W272R)
ISCN -
DB-ID C7orf50_000005
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPER NM_001039966.1 ?/. - c.814T>C r.(?) p.(Trp272Arg)
C7orf50 NM_032350.5 ?/. - c.129+34715A>G r.(=) p.(=)
GPR146 NM_138445.2 ?/. - c.*34025T>C r.(=) p.(=)


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