Variant #0000267196 (NC_000020.10:g.44523782C>T, NM_001278535.1:c.-4152G>A (NEURL2))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44523782C>T
DNA change (hg38) g.45895143C>T
Published as CTSA(NM_001127695.2):c.1088+10C>T, CTSA(NM_001127695.3):c.1088+10C>T
ISCN -
DB-ID CTSA_000012 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) 0.66499 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.1142+10C>T r.(=) p.(=)
NEURL2 NM_001278535.1 -/. - c.-4152G>A r.(?) p.(=)
PLTP NM_006227.3 -/. - c.*3798G>A r.(=) p.(=)


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