Variant #0000621183 (NC_000003.11:g.133119173T>C, BFSP2(NM_003571.2):c.246T>C)

Chromosome 3
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.133119173T>C
DNA change (hg38) g.133400329T>C
Published as BFSP2(NM_003571.3):c.246T>C (p.S82=)
ISCN -
DB-ID BFSP2_000009
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) 0.00166 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-15 15:34:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BFSP2 NM_003571.2 -?/. - c.246T>C r.(?) p.(Ser82=)
TMEM108 NM_023943.2 -?/. - c.*4343T>C r.(=) p.(=)