Variant #0000518311 (NC_000003.11:g.15084335T>G, NM_022497.3:c.*9613A>C (MRPS25))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15084335T>G
DNA change (hg38) g.15042828T>G
Published as NR2C2(NM_003298.3):c.1674-6T>G (p.(=))
ISCN -
DB-ID MRPS25_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR2C2 NM_003298.3 -?/. - c.1674-6T>G r.(=) p.(=)
MRPS25 NM_022497.3 -?/. - c.*9613A>C r.(=) p.(=)


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