Variant #0000807928 (NC_000017.10:g.37821613A>G, NM_003673.3:c.1A>G (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.37821613A>G
DNA change (hg38) -
Published as TCAP(NM_003673.3):c.1A>G (p.M1?)
ISCN -
DB-ID PNMT_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STARD3 NM_001165937.1 ?/. - c.*2452A>G r.(=) p.(=)
PNMT NM_002686.3 ?/. - c.-3116A>G r.(?) p.(=)
TCAP NM_003673.3 ?/. - c.1A>G r.(?) p.(Met1?)


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