Variant #0000321826 (NC_000010.10:g.135236970_135236981del, NM_138384.2:c.*3301_*3312del (MTG1))

Chromosome 10
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.135236970_135236981del
DNA change (hg38) g.133423466_133423477del
Published as SPRN(NM_001012508.3):c.216_227del (p.?), SPRN(NM_001012508.3):c.216_227delAGCCGGGGCGGC (p.A79_G82del)
ISCN -
DB-ID SPRN_000001 See all 2 reported entries
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPRN NM_001012508.3 ?/. - c.216_227del r.(?) p.(Ala79_Gly82del)
MTG1 NM_138384.2 ?/. - c.*3301_*3312del r.(=) p.(=)


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