Variant #0000575052 (NC_000023.10:g.154743837T>A, NM_018196.3:c.448A>T (TMLHE))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.154743837T>A
DNA change (hg38) g.155514176T>A
Published as TMLHE(NM_018196.3):c.448A>T (p.(Ile150Leu)), TMLHE(NM_018196.4):c.448A>T (p.I150L)
ISCN -
DB-ID TMLHE_000026 See all 2 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) 0.00025 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.448A>T r.(?) p.(Ile150Leu)


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