Variant #0000561215 (NC_000017.10:g.37821649_37821651del, NM_003673.3:c.37_39del (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.37821649_37821651del
DNA change (hg38) g.39665396_39665398del
Published as TCAP(NM_003673.3):c.37_39del (p.(Glu13del)), TCAP(NM_003673.3):c.37_39delGAG (p.E13del), TCAP(NM_003673.4):c.37_39delGAG (p.E13del)
ISCN -
DB-ID TCAP_000010 See all 18 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.*2488_*2490del r.(=) p.(=)
PNMT NM_002686.3 -?/. - c.-3080_-3078del r.(?) p.(=)
TCAP NM_003673.3 -?/. - c.37_39del r.(?) p.(Glu13del)


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