Variant #0000541097 (NC_000010.10:g.81841430_81841431dup, NC_000010.10(NM_025125.3):c.88-167_88-166dup (TMEM254))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.81841430_81841431dup
DNA change (hg38) g.80081674_80081675dup
Published as TMEM254(NM_001270374.1):c.47_48dupAA (p.E17Kfs*6)
ISCN -
DB-ID TMEM254_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
TMEM254 NM_025125.3 -/. - c.88-167_88-166dup r.(=) p.(=)


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