Variant #0000535039 (NC_000008.10:g.59492223G>C, NM_003580.3:c.*4442C>G (NSMAF))

Chromosome 8
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.59492223G>C
DNA change (hg38) g.58579664G>C
Published as SDCBP(NM_001330537.1):c.680G>C (p.G227A)
ISCN -
DB-ID NSMAF_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) Retrieve
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NSMAF NM_003580.3 ?/. - c.*4442C>G r.(=) p.(=)
SDCBP NM_005625.3 ?/. - c.620G>C r.(?) p.(Gly207Ala)


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