Variant #0000624107 (NC_000019.9:g.7695706C>G, NC_000019.9(NM_001171155.1):c.115-3C>G (PET100))

Chromosome 19
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.7695706C>G
DNA change (hg38) g.7630820C>G
Published as PET100(NM_001171155.1):c.115-3C>G
ISCN -
DB-ID PET100_000010
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) 1.0E-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 2019-12-06 12:43:26 +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     
PET100 NM_001171155.1 ?/. - c.115-3C>G r.spl? p.?
XAB2 NM_020196.2 ?/. - c.-1293G>C r.(?) p.(=)
PCP2 NM_174895.1 ?/. - c.*869G>C r.(=) p.(=)


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