Variant #0000313171 (NC_000017.10:g.80788465T>C, NC_000017.10(NM_005993.4):c.1318+15655T>C (TBCD))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.80788465T>C
DNA change (hg38) g.82830589T>C
Published as TBCD(NM_005993.5):c.1318+15655T>C, ZNF750(NM_024702.3):c.1725A>G (p.A575=)
ISCN -
DB-ID TBCD_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) 0.39277 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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     
TBCD NM_005993.4 -/. - c.1318+15655T>C r.(=) p.(=)
ZNF750 NM_024702.2 -/. - c.1725A>G r.(?) p.(Ala575=)


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