Variant #0000659132 (NC_000023.10:g.149765043C>T, NC_000023.10(NM_000252.2):c.136+9C>T (MTM1))

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.149765043C>T
DNA change (hg38) g.150596579C>T
Published as MTM1(NM_000252.2):c.136+9C>T, MTM1(NM_000252.3):c.136+9C>T
ISCN -
DB-ID MTM1_000333 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 -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00076 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTM1 NM_000252.2 -/. - c.136+9C>T r.(=) p.(=)


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