Variant #0000718356 (NC_000002.11:g.1914112C>T, NM_015025.2:c.1711G>A (MYT1L))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1914112C>T
DNA change (hg38) -
Published as MYT1L(NM_001329851.3):c.1717G>A (p.G573R), MYT1L(NM_015025.4):c.1711G>A (p.G571R)
ISCN -
DB-ID MYT1L_000038 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) 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYT1L NM_015025.2 +?/. - c.1711G>A r.(?) p.(Gly571Arg)


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