Variant #0000808389 (NC_000018.9:g.19085529G>C, NC_000018.9(NM_001142966.1):c.4228+1G>C (GREB1L))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19085529G>C
DNA change (hg38) -
Published as GREB1L(NM_001142966.2):c.4228+1G>C, GREB1L(NM_001142966.3):c.4228+1G>C
ISCN -
DB-ID GREB1L_000038 See all 2 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GREB1L NM_001142966.1 +?/. - c.4228+1G>C r.spl? p.?


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