Variant #0000534707 (NC_000008.10:g.37594198T>C, NC_000008.10(NM_007175.6):c.-16+2T>C (ERLIN2))

Chromosome 8
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.37594198T>C
DNA change (hg38) g.37736680T>C
Published as ERLIN2(NM_001003790.3):c.-343T>C (p.(=))
ISCN -
DB-ID ERLIN2_000006
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 2020-06-23 18:59:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERLIN2 NM_007175.6 ?/. - c.-16+2T>C r.spl? p.?


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