Variant #0000855051 (NC_000017.10:g.61899394T>C, NM_002805.5:c.-5457T>C (PSMC5))

Chromosome 17
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.61899394T>C
DNA change (hg38) -
Published as FTSJ3(NM_017647.4):c.1425A>G (p.P475=)
ISCN -
DB-ID FTSJ3_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC5 NM_002805.5 -?/. - c.-5457T>C r.(?) p.(=)
FTSJ3 NM_017647.3 -?/. - c.1425A>G r.(?) p.(Pro475=)


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