Variant #0000291817 (NC_000023.10:g.10491233C>A, MID1(NM_000381.3):c.661-6G>T)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10491233C>A
DNA change (hg38) g.10523193C>A
Published as MID1(NM_000381.3):c.661-6G>T, MID1(NM_000381.3):c.661-6delinsT (p.(=)), MID1(NM_000381.4):c.661-6G>T
ISCN -
DB-ID MID1_000031 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MID1 NM_000381.3 -/. - c.661-6G>T r.(=) p.(=)