Variant #0000570140 (NC_000020.10:g.60714187C>G, NM_198935.1:c.-4690C>G (SS18L1))

Chromosome 20
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.60714187C>G
DNA change (hg38) g.62139131C>G
Published as PSMA7(NM_002792.3):c.415G>C (p.(Asp139His))
ISCN -
DB-ID LSM14B_000002
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 View details
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     
PSMA7 NM_002792.3 ?/. - c.415G>C r.(?) p.(Asp139His)
LSM14B NM_144703.2 ?/. - c.*4983C>G r.(=) p.(=)
SS18L1 NM_198935.1 ?/. - c.-4690C>G r.(?) p.(=)


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