Variant #0000329825 (NC_000004.11:g.2933283C>T, NM_014189.3:c.*3033C>T (ADD1))

Chromosome 4
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.2933283C>T
DNA change (hg38) g.2931556C>T
Published as MFSD10(NM_001120.4):c.1022G>A (p.(Arg341Gln))
ISCN -
DB-ID MFSD10_000001
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) 7.0E-5 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     
MFSD10 NM_001120.4 ?/. - c.1022G>A r.(?) p.(Arg341Gln)
NOP14 NM_003703.1 ?/. - c.*6652G>A r.(=) p.(=)
ADD1 NM_014189.3 ?/. - c.*3033C>T r.(=) p.(=)


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