Variant #0000855852 (NC_000020.10:g.44519429C>A, NM_001278535.1:c.202G>T (NEURL2))

Chromosome 20
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.44519429C>A
DNA change (hg38) -
Published as NEURL2(NM_001278535.1):c.202G>T (p.(Val68Phe))
ISCN -
DB-ID CTSA_000043
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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSA NM_000308.2 ?/. - c.-536C>A r.(?) p.(=)
NEURL2 NM_001278535.1 ?/. - c.202G>T r.(?) p.(Val68Phe)
PLTP NM_006227.3 ?/. - c.*8151G>T r.(=) p.(=)
SPATA25 NM_080608.3 ?/. - c.-3200G>T r.(?) p.(=)


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