Variant #0000721965 (NC_000008.10:g.37620276G>T, NM_007198.3:c.99G>T (PROSC))

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.37620276G>T
DNA change (hg38) -
Published as PLPBP(NM_001349346.1):c.99G>T (p.R33=)
ISCN -
DB-ID ERLIN2_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERLIN2 NM_007175.6 ?/. - c.*8643G>T r.(=) p.(=)
PROSC NM_007198.3 ?/. - c.99G>T r.(?) p.(Arg33=)


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