Variant #0000680969 (NC_000017.10:g.61912911C>T, NM_002805.5:c.*3582C>T (PSMC5))

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.61912911C>T
DNA change (hg38) -
Published as SMARCD2(NM_001098426.1):c.584G>A (p.R195Q)
ISCN -
DB-ID FTSJ3_000007
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCD2 NM_001098426.1 ?/. - c.584G>A r.(?) p.(Arg195Gln)
PSMC5 NM_002805.5 ?/. - c.*3582C>T r.(=) p.(=)
FTSJ3 NM_017647.3 ?/. - c.-8526G>A r.(?) p.(=)


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