Variant #0000532435 (NC_000007.13:g.6523655G>C, NM_006854.3:c.34C>G (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.6523655G>C
DNA change (hg38) g.6484024G>C
Published as KDELR2(NM_001100603.1):c.34C>G (p.(His12Asp)), KDELR2(NM_006854.4):c.34C>G (p.H12D)
ISCN -
DB-ID KDELR2_000002 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDELR2 NM_001100603.1 ?/. - c.34C>G r.(?) p.(His12Asp)
KDELR2 NM_006854.3 ?/. - c.34C>G r.(?) p.(His12Asp)


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