Variant #0000330397 (NC_000005.9:g.61714955G>T, NM_014473.2:c.-15356C>A (DIMT1))

Chromosome 5
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.61714955G>T
DNA change (hg38) g.62419128G>T
Published as IPO11(NM_001134779.1):c.114+1G>T (p.?)
ISCN -
DB-ID IPO11_000001
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) 0.0001 View details
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 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     
DIMT1 NM_014473.2 ?/. - c.-15356C>A r.(?) p.(=)
IPO11 NM_016338.4 ?/. - c.-7+6199G>T r.(=) p.(=)
LRRC70 NM_181506.4 ?/. - c.-159846G>T r.(?) p.(=)


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