Variant #0000977801 (NC_000007.13:g.6505921C>G, NM_006854.3:c.385G>C (KDELR2))

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.6505921C>G
DNA change (hg38) -
Published as KDELR2(NM_006854.4):c.385G>C (p.(Val129Leu))
ISCN -
DB-ID KDELR2_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDELR2 NM_001100603.1 ?/. - c.352-3115G>C r.(=) p.(=)
KDELR2 NM_006854.3 ?/. - c.385G>C r.(?) p.(Val129Leu)


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