Variant #0000563794 (NC_000017.10:g.80899349T>C, NM_005993.4:c.3554T>C (TBCD))

Chromosome 17
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.80899349T>C
DNA change (hg38) g.82941473T>C
Published as TBCD(NM_005993.4):c.3554T>C (p.(Leu1185Pro))
ISCN -
DB-ID B3GNTL1_000002
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) 0.00599 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
B3GNTL1 NM_001009905.1 -?/. - c.*2601A>G r.(=) p.(=)
TBCD NM_005993.4 -?/. - c.3554T>C r.(?) p.(Leu1185Pro)
ZNF750 NM_024702.2 -?/. - c.-101729A>G r.(?) p.(=)


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