Variant #0000575046 (NC_000023.10:g.154721305C>T, NM_018196.3:c.1157G>A (TMLHE))

Chromosome X
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.154721305C>T
DNA change (hg38) g.155491644C>T
Published as TMLHE(NM_018196.3):c.1157G>A (p.R386H)
ISCN -
DB-ID TMLHE_000022
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) 6.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMLHE NM_018196.3 ?/. - c.1157G>A r.(?) p.(Arg386His)
TMLHE-AS1 NR_039991.1 ?/. - n.472-1236C>T r.(?) -


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