Variant #0000441441 (NC_000003.11:g.14170833_14170834dup, NC_000003.11(NM_024334.2):c.13-79_13-78dup (TMEM43))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.14170833_14170834dup
DNA change (hg38) g.14129333_14129334dup
Published as 13-93_13-94insAA
ISCN -
DB-ID TMEM43_000001 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs10648308
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 10:28:37 +01:00 (CET)
Date last edited 2018-12-24 15:13:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TMEM43 NM_024334.2 -/- 1i c.13-79_13-78dup r.(=) p.(=) -


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