Variant #0000556600 (NC_000016.9:g.1394279C>T, NM_001199096.1:c.1455C>T (BAIAP3))

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.1394279C>T
DNA change (hg38) g.1344278C>T
Published as BAIAP3(NM_003933.4):c.1668C>T (p.F556=)
ISCN -
DB-ID BAIAP3_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) Retrieve
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 2020-07-07 12:44:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSR3 NM_001001410.2 -?/. - c.*5159G>A r.(=) p.(=)
BAIAP3 NM_001199096.1 -?/. - c.1455C>T r.(?) p.(Phe485=)


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