Variant #0000329634 (NC_000003.11:g.135870731G>C, NM_002718.4:c.*6723G>C (PPP2R3A))

Chromosome 3
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.135870731G>C
DNA change (hg38) g.136151889G>C
Published as MSL2(NM_001145417.1):c.770C>G (p.(Ala257Gly))
ISCN -
DB-ID MSL2_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) 0.0005 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 2018-01-15 20:58:59 +01:00 (CET)
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     
PPP2R3A NM_002718.4 ?/. - c.*6723G>C r.(=) p.(=)
MSL2 NM_018133.3 ?/. - c.992C>G r.(?) p.(Ala331Gly)


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