Variant #0000689169 (NC_000004.11:g.100485262A>C, NM_000253.2:c.-234A>C (MTTP))

Chromosome 4
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.100485262A>C
DNA change (hg38) -
Published as MTTP(NM_001300785.1):c.10A>C (p.R4=)
ISCN -
DB-ID MTTP_000257
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTTP NM_000253.2 -?/. - c.-234A>C r.(?) p.(=)
TRMT10A NM_152292.4 -?/. - c.-750T>G r.(?) p.(=)


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