Variant #0000691958 (NC_000016.9:g.175094_175096del, NC_000016.9(NM_001077350.2):c.188+5443_188+5445del (NPRL3))

Chromosome 16
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.175094_175096del
DNA change (hg38) -
Published as NPRL3(NM_001077350.3):c.188+5443_188+5445delTTT
ISCN -
DB-ID MPG_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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +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     
MPG NM_001015052.2 -/. - c.*39318_*39320del r.(=) p.(=)
NPRL3 NM_001077350.2 -/. - c.188+5443_188+5445del r.(=) p.(=)


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