Variant #0000561219 (NC_000017.10:g.37821770C>T, NC_000017.10(NM_003673.3):c.110+48C>T (TCAP))

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.37821770C>T
DNA change (hg38) g.39665517C>T
Published as -
ISCN -
DB-ID TCAP_000024 See all 2 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) 0.03892 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.*2609C>T r.(=) p.(=)
PNMT NM_002686.3 -/. - c.-2959C>T r.(?) p.(=)
TCAP NM_003673.3 -/. - c.110+48C>T r.(=) p.(=)


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