Variant #0000331368 (NC_000007.13:g.1097814C>A, NC_000007.13(NM_032350.5):c.130-48035G>T (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.1097814C>A
DNA change (hg38) g.1058178C>A
Published as C7orf50(NM_001134395.1):c.130-48035G>T (p.(=))
ISCN -
DB-ID C7orf50_000003
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) 0.00079 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPER NM_001039966.1 ?/. - c.-29513C>A r.(?) p.(=)
C7orf50 NM_032350.5 ?/. - c.130-48035G>T r.(=) p.(=)
GPR146 NM_138445.2 ?/. - c.663C>A r.(?) p.(Asp221Glu)


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