Variant #0000970589 (NC_000023.10:g.10491249dup, NC_000023.10(NM_000381.3):c.661-7dup (MID1))

Chromosome X
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.10491249dup
DNA change (hg38) -
Published as MID1(NM_000381.3):c.661-7dup (p.(=)), MID1(NM_000381.4):c.661-7dupT, MID1(NM_001347733.1):c.661-7dupT, MID1(NM_001347733.2):c.661-7dupT
ISCN -
DB-ID MID1_000005 See all 5 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MID1 NM_000381.3 -?/. - c.661-7dup r.(=) p.(=)


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