Variant #0000331119 (NC_000006.11:g.90372565_90372576del, NM_014611.1:c.14361_14372del (MDN1))

Chromosome 6
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.90372565_90372576del
DNA change (hg38) g.89662846_89662857del
Published as MDN1(NM_014611.1):c.14361_14372del (p.?)
ISCN -
DB-ID MDN1_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_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     
MDN1 NM_014611.1 ?/. - c.14361_14372del r.(?) p.(Asp4787_Glu4790del)
LYRM2 NM_020466.4 ?/. - c.-24127_-24116del r.(?) p.(=)


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