Variant #0000520910 (NC_000004.11:g.100485284G>A, NM_000253.2:c.-212G>A (MTTP))

Chromosome 4
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.100485284G>A
DNA change (hg38) g.99564127G>A
Published as MTTP(NM_000253.4):c.-212G>A, MTTP(NM_001300785.1):c.32G>A (p.R11Q), TRMT10A(NM_152292.5):c.-772C>T
ISCN -
DB-ID MTTP_000102 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) 0.00023 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTTP NM_000253.2 ?/. - c.-212G>A r.(?) p.(=)
TRMT10A NM_152292.4 ?/. - c.-772C>T r.(?) p.(=)


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