Variant #0000517996 (NC_000003.11:g.133119151G>A, BFSP2(NM_003571.2):c.224G>A)

Chromosome 3
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.133119151G>A
DNA change (hg38) g.133400307G>A
Published as BFSP2(NM_003571.2):c.224G>A (p.(Arg75His))
ISCN -
DB-ID BFSP2_000006
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BFSP2 NM_003571.2 ?/. - c.224G>A r.(?) p.(Arg75His)
TMEM108 NM_023943.2 ?/. - c.*4321G>A r.(=) p.(=)