Variant #0000561231 (NC_000017.10:g.37822171G>C, NM_003673.3:c.313G>C (TCAP))

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.37822171G>C
DNA change (hg38) g.39665918G>C
Published as TCAP(NM_003673.3):c.313G>C (p.E105Q, p.(Glu105Gln)), TCAP(NM_003673.4):c.313G>C (p.E105Q)
ISCN -
DB-ID TCAP_000069 See all 12 reported entries
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) 0.0005 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 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     
STARD3 NM_001165937.1 ?/. - c.*3010G>C r.(=) p.(=)
PNMT NM_002686.3 ?/. - c.-2558G>C r.(?) p.(=)
TCAP NM_003673.3 ?/. - c.313G>C r.(?) p.(Glu105Gln)


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