Variant #0000267197 (NC_000020.10:g.44526676G>A, NM_001278535.1:c.-7046C>T (NEURL2))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44526676G>A
DNA change (hg38) g.45898037G>A
Published as CTSA(NM_000308.2):c.1341G>A (p.(Lys447=)), CTSA(NM_001127695.3):c.1287G>A (p.K429=)
ISCN -
DB-ID CTSA_000013 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) 0.00284 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSA NM_000308.2 -?/. - c.1341G>A r.(?) p.(Lys447=)
NEURL2 NM_001278535.1 -?/. - c.-7046C>T r.(?) p.(=)
PLTP NM_006227.3 -?/. - c.*904C>T r.(=) p.(=)


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