Variant #0000247863 (NC_000019.9:g.18980213A>G, NC_000019.9(NM_001492.4):c.326-14T>C (GDF1))

Chromosome 19
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.18980213A>G
DNA change (hg38) g.18869404A>G
Published as CERS1(NM_021267.5):c.*595-14T>C, GDF1(NM_001492.5):c.326-14T>C, GDF1(NM_001492.6):c.326-14T>C
ISCN -
DB-ID GDF1_000007 See all 4 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) 0.99993 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
GDF1 NM_001492.4 -/. - c.326-14T>C r.(=) p.(=)
UPF1 NM_002911.3 -/. - c.*2887A>G r.(=) p.(=)
CERS1 NM_021267.3 -/. - c.*595-14T>C r.(=) p.(=)


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