Variant #0000948865 (NC_000007.13:g.142640916G>A, NM_000420.2:c.1546C>T (KEL))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.142640916G>A
DNA change (hg38) -
Published as KEL(NM_000420.3):c.1546C>T (p.R516*)
ISCN -
DB-ID C7orf34_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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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     
KEL NM_000420.2 +/. - c.1546C>T r.(?) p.(Arg516*)
C7orf34 NM_178829.4 +/. - c.*3242G>A r.(=) p.(=)


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