Variant #0000852177 (NC_000009.11:g.139317609_139317616del, NM_006643.3:c.-12767_-12760del (SDCCAG3))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.139317609_139317616del
DNA change (hg38) -
Published as PMPCA(NM_015160.3):c.1471_1478delGTGGCCGC (p.V491Pfs*3)
ISCN -
DB-ID PMPCA_000021
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SDCCAG3 NM_006643.3 +?/. - c.-12767_-12760del r.(?) p.(=)
PMPCA NM_015160.1 +?/. - c.1471_1478del r.(?) p.(Val491Profs*3)


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