Variant #0000522520 (NC_000004.11:g.38016365_38016367del, NM_015173.3:c.653_655del (TBC1D1))

Chromosome 4
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.38016365_38016367del
DNA change (hg38) g.38014744_38014746del
Published as TBC1D1(NM_001253912.1):c.653_655del (p.(His218_Ala219delinsPro))
ISCN -
DB-ID PTTG2_000003
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_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     
PTTG2 NM_006607.2 -?/. - c.*53734_*53736del r.(=) p.(=)
TBC1D1 NM_015173.3 -?/. - c.653_655del r.(?) p.(His218_Ala219delinsPro)


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