Variant #0000726322 (NC_000017.10:g.37822066C>T, NM_003673.3:c.208C>T (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.37822066C>T
DNA change (hg38) -
Published as TCAP(NM_003673.3):c.208C>T (p.R70W), TCAP(NM_003673.4):c.208C>T (p.R70W)
ISCN -
DB-ID TCAP_000011 See all 8 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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +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     
STARD3 NM_001165937.1 ?/. - c.*2905C>T r.(=) p.(=)
PNMT NM_002686.3 ?/. - c.-2663C>T r.(?) p.(=)
TCAP NM_003673.3 ?/. - c.208C>T r.(?) p.(Arg70Trp)


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