Variant #0000894366 (NC_000017.10:g.80897245C>G, NM_005993.4:c.3372C>G (TBCD))

Chromosome 17
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.80897245C>G
DNA change (hg38) -
Published as TBCD(NM_005993.5):c.3372C>G (p.I1124M)
ISCN -
DB-ID B3GNTL1_000001
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GNTL1 NM_001009905.1 ?/. - c.*4705G>C r.(=) p.(=)
TBCD NM_005993.4 ?/. - c.3372C>G r.(?) p.(Ile1124Met)
ZNF750 NM_024702.2 ?/. - c.-99625G>C r.(?) p.(=)


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