Variant #0000566937 (NC_000019.9:g.3557401T>C, NM_001135580.1:c.*13393T>C (C19orf71))

Chromosome 19
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.3557401T>C
DNA change (hg38) g.3557403T>C
Published as MFSD12(NM_174983.5):c.1A>G (p.M1?)
ISCN -
DB-ID C19orf71_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) 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 2020-07-15 10:03:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf71 NM_001135580.1 ?/. - c.*13393T>C r.(=) p.(=)
MFSD12 NM_174983.3 ?/. - c.1A>G r.(?) p.(Met1?)


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