Variant #0000610650 (NC_000007.13:g.11871501_11871506dup, NM_015204.2:c.71_76dup (THSD7A))

Chromosome 7
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.11871501_11871506dup
DNA change (hg38) g.11831875_11831880dup
Published as THSD7A(NM_015204.2):c.76_77insAGCTGC (p.(Gln24_Leu25dup))
ISCN -
DB-ID THSD7A_000010
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THSD7A NM_015204.2 -?/. - c.71_76dup r.(?) p.(Gln24_Leu25dup)


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