Variant #0000330034 (NC_000004.11:g.84374915T>C, NM_139076.2:c.*8707A>G (FAM175A))

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.84374915T>C
DNA change (hg38) g.83453762T>C
Published as HELQ(NM_133636.2):c.481A>G (p.(Thr161Ala))
ISCN -
DB-ID HELQ_000001
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS18C NM_016067.2 ?/. - c.-2316T>C r.(?) p.(=)
HELQ NM_133636.2 ?/. - c.481A>G r.(?) p.(Thr161Ala)
FAM175A NM_139076.2 ?/. - c.*8707A>G r.(=) p.(=)


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