Variant #0000535319 (NC_000008.10:g.74893388_74893390del, NC_000008.10(NM_017866.5):c.317-2_317del (TMEM70))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74893388_74893390del
DNA change (hg38) g.73981153_73981155del
Published as TMEM70(NM_001040613.2):c.*7-2_*7del (p.(=))
ISCN -
DB-ID TMEM70_000013
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-24 13:58:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM70 NM_017866.5 -?/. - c.317-2_317del r.spl? p.?


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