Variant #0000725244 (NC_000015.9:g.65313871G>A, NM_139242.3:c.626C>T (MTFMT))

Chromosome 15
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.65313871G>A
DNA change (hg38) -
Published as MTFMT(NM_139242.3):c.626C>T (p.S209L), MTFMT(NM_139242.4):c.626C>T (p.S209L)
ISCN -
DB-ID MTFMT_000004 See all 9 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) 0.00034 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTFMT NM_139242.3 ?/. - c.626C>T r.(?) p.(Ser209Leu)


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