Variant #0000562635 (NC_000017.10:g.61911851G>A, NM_002805.5:c.*2522G>A (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.61911851G>A
DNA change (hg38) g.63834491G>A
Published as SMARCD2(NM_001098426.1):c.904C>T (p.L302F)
ISCN -
DB-ID FTSJ3_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) 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 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     
SMARCD2 NM_001098426.1 -?/. - c.904C>T r.(?) p.(Leu302Phe)
PSMC5 NM_002805.5 -?/. - c.*2522G>A r.(=) p.(=)
FTSJ3 NM_017647.3 -?/. - c.-7466C>T r.(?) p.(=)


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