Variant #0000537170 (NC_000009.11:g.139316420C>T, NM_006643.3:c.-11571G>A (SDCCAG3))

Chromosome 9
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.139316420C>T
DNA change (hg38) g.136421968C>T
Published as PMPCA(NM_015160.2):c.1400C>T (p.T467M)
ISCN -
DB-ID PMPCA_000009
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) 3.0E-5 View details
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     
SDCCAG3 NM_006643.3 -?/. - c.-11571G>A r.(?) p.(=)
PMPCA NM_015160.1 -?/. - c.1400C>T r.(?) p.(Thr467Met)


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