Variant #0000263692 (NC_000003.11:g.133119306C>G, NM_003571.2:c.379C>G (BFSP2))

Chromosome 3
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.133119306C>G
DNA change (hg38) g.133400462C>G
Published as BFSP2(NM_003571.3):c.379C>G (p.Q127E)
ISCN -
DB-ID BFSP2_000021
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) 0.0009 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-11 21:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BFSP2 NM_003571.2 -/. - c.379C>G r.(?) p.(Gln127Glu)
TMEM108 NM_023943.2 -/. - c.*4476C>G r.(=) p.(=)


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