Variant #0000923796 (NC_000002.11:g.96931092del, NM_017849.3:c.30del (TMEM127))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.96931092del
DNA change (hg38) -
Published as TMEM127(NM_017849.4):c.30delC (p.G11Afs*70)
ISCN -
DB-ID CIAO1_000014
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CIAO1 NM_004804.2 +/. - c.-997del r.(?) p.(=)
TMEM127 NM_017849.3 +/. - c.30del r.(?) p.(Gly11Alafs*70)


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