Variant #0000304425 (NC_000014.8:g.74959922G>T, NM_000428.2:c.*7665C>A (LTBP2))

Chromosome 14
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.74959922G>T
DNA change (hg38) g.74493219G>T
Published as NPC2(NM_006432.4):c.56C>A (p.A19D)
ISCN -
DB-ID NPC2_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) 5.0E-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 2018-01-15 20:58:59 +01:00 (CET)
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.*7665C>A r.(=) p.(=)
NPC2 NM_006432.3 ?/. - c.56C>A r.(?) p.(Ala19Asp)
ISCA2 NM_194279.2 ?/. - c.-556G>T r.(?) p.(=)


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