Variant #0000615704 (NC_000016.9:g.14723963C>G, NC_000016.9(NM_002582.3):c.19+1G>C (PARN))

Chromosome 16
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.14723963C>G
DNA change (hg38) g.14630106C>G
Published as PARN(NM_002582.4):c.19+1G>C
ISCN -
DB-ID BFAR_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-09 13:33:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PARN NM_002582.3 +/. - c.19+1G>C r.spl? p.?
BFAR NM_016561.2 +/. - c.-2986C>G r.(?) p.(=)


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