Variant #0000928172 (NC_000001.10:g.38273851A>C, NM_005955.2:c.*6957T>G (MTF1))

Chromosome 1
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.38273851A>C
DNA change (hg38) -
Published as YRDC(NM_024640.4):c.2T>G (p.M1?)
ISCN -
DB-ID C1orf122_000005
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTF1 NM_005955.2 ?/. - c.*6957T>G r.(=) p.(=)
YRDC NM_024640.3 ?/. - c.2T>G r.(?) p.?
C1orf122 NM_198446.2 ?/. - c.-226A>C r.(?) p.(=)


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