Variant #0000615930 (NC_000016.9:g.30038021G>A, NM_031478.4:c.353C>T (FAM57B))

Chromosome 16
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.30038021G>A
DNA change (hg38) g.30026700G>A
Published as FAM57B(NM_031478.5):c.353C>T (p.T118M)
ISCN -
DB-ID FAM57B_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) 7.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C16orf92 NM_001109659.1 -?/. - c.*2473G>A r.(=) p.(=)
FAM57B NM_031478.4 -?/. - c.353C>T r.(?) p.(Thr118Met)


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