Variant #0000924240 (NC_000005.9:g.132197286G>A, NM_005260.3:c.1360C>T (GDF9))

Chromosome 5
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.132197286G>A
DNA change (hg38) -
Published as GDF9(NM_005260.7):c.1360C>T (p.R454C)
ISCN -
DB-ID GDF9_000003
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) 0.00298 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF9 NM_005260.3 ?/. - c.1360C>T r.(?) p.(Arg454Cys)
UQCRQ NM_014402.4 ?/. - c.-5107G>A r.(?) p.(=)


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