Variant #0000249260 (NC_000020.10:g.60712511A>G, NC_000020.10(NM_002792.3):c.592-29T>C (PSMA7))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.60712511A>G
DNA change (hg38) g.62137455A>G
Published as PSMA7(NM_002792.4):c.592-29T>C
ISCN -
DB-ID PSMA7_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) 0.76854 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMA7 NM_002792.3 -/. - c.592-29T>C r.(=) p.(=)
LSM14B NM_144703.2 -/. - c.*3307A>G r.(=) p.(=)


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