Variant #0000553002 (NC_000014.8:g.74959920C>A, NM_000428.2:c.*7667G>T (LTBP2))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74959920C>A
DNA change (hg38) g.74493217C>A
Published as NPC2(NM_006432.4):c.58G>T (p.E20*)
ISCN -
DB-ID NPC2_000016 See all 13 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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP2 NM_000428.2 +/. - c.*7667G>T r.(=) p.(=)
NPC2 NM_006432.3 +/. - c.58G>T r.(?) p.(Glu20Ter)
ISCA2 NM_194279.2 +/. - c.-558C>A r.(?) p.(=)


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