Variant #0000948261 (NC_000004.11:g.128843076T>C, NM_152778.2:c.1041A>G (MFSD8))

Chromosome 4
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.128843076T>C
DNA change (hg38) -
Published as MFSD8(NM_152778.2):c.1041A>G (p.V347=), MFSD8(NM_152778.3):c.1041A>G (p.V347=), MFSD8(NM_152778.4):c.1041A>G (p.V347=)
ISCN -
DB-ID C4orf29_000005 See all 3 reported entries
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) 0.00072 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf29 NM_001039717.1 -?/. - c.-43703T>C r.(?) p.(=)
MFSD8 NM_152778.2 -?/. - c.1041A>G r.(?) p.(Val347=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.