Variant #0000441445 (NC_000003.11:g.?, NC_000003.11(NM_024334.2):c.163-22_163-23insC (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.?
DNA change (hg38) -
Published as -
ISCN -
DB-ID TMEM43_000005
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35334148
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 10:33:27 +01:00 (CET)
Date last edited 2018-12-24 15:05:57 +01:00 (CET)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TMEM43 NM_024334.2 -/- 2i c.163-22_163-23insC r.(?) p.(=) -


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