Variant #0000311754 (NC_000017.10:g.37821953C>G, NC_000017.10(NM_003673.3):c.111-16C>G (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.37821953C>G
DNA change (hg38) g.39665700C>G
Published as TCAP(NM_003673.3):c.111-16C>G, TCAP(NM_003673.4):c.111-16C>G
ISCN -
DB-ID TCAP_000046 See all 3 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) 0.00041 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STARD3 NM_001165937.1 -?/. - c.*2792C>G r.(=) p.(=)
PNMT NM_002686.3 -?/. - c.-2776C>G r.(?) p.(=)
TCAP NM_003673.3 -?/. - c.111-16C>G r.(=) p.(=)


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