Variant #0000521656 (NC_000004.11:g.128843076T>C, NM_152778.2:c.1041A>G (MFSD8))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128843076T>C
DNA change (hg38) g.127921921T>C
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_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 2023-11-27 17:27:23 +01:00 (CET)
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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=)


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