Variant #0000886270 (NC_000004.11:g.38016360G>C, NM_015173.3:c.648G>C (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.38016360G>C
DNA change (hg38) -
Published as TBC1D1(NM_015173.4):c.648G>C (p.P216=)
ISCN -
DB-ID PTTG2_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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTTG2 NM_006607.2 -?/. - c.*53729G>C r.(=) p.(=)
TBC1D1 NM_015173.3 -?/. - c.648G>C r.(?) p.(Pro216=)


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