Variant #0000616483 (NC_000017.10:g.37821644C>T, NM_003673.3:c.32C>T (TCAP))

Chromosome 17
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.37821644C>T
DNA change (hg38) g.39665391C>T
Published as TCAP(NM_003673.3):c.32C>T (p.S11L), TCAP(NM_003673.4):c.32C>T (p.S11L)
ISCN -
DB-ID TCAP_000038 See all 4 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) 0.00025 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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.*2483C>T r.(=) p.(=)
PNMT NM_002686.3 -?/. - c.-3085C>T r.(?) p.(=)
TCAP NM_003673.3 -?/. - c.32C>T r.(?) p.(Ser11Leu)


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