Variant #0000853210 (NC_000011.9:g.85346825_85346826insTCATACCGTTCCACTGCCACCAAA, NC_000011.9(NM_018480.4):c.509+3_509+4insTCATACCGTTCCACTGCCACCAAA (TMEM126B))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.85346825_85346826insTCATACCGTTCCACTGCCACCAAA
DNA change (hg38) -
Published as TMEM126B(NM_001193538.3):c.419+2_419+3insATCATACCGTTCCACTGCCACCAA
ISCN -
DB-ID TMEM126B_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:40:45 +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     
TMEM126B NM_018480.4 ?/. - c.509+3_509+4insTCATACCGTTCCACTGCCACCAAA r.spl? p.?


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