Variant #0001066589 (NC_000017.10:g.648438G>A, NM_015721.2:c.2845C>T (GEMIN4))

Chromosome 17
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.648438G>A
DNA change (hg38) -
Published as GEMIN4(NM_015721.3):c.2845C>T (p.(Arg949Cys))
ISCN -
DB-ID FAM57A_000013
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) 0.00055 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GEMIN4 NM_015721.2 ?/. - c.2845C>T r.(?) p.(Arg949Cys)
FAM57A NM_024792.1 ?/. - c.*3628G>A r.(=) p.(=)


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