Variant #0000320746 (NC_000001.10:g.38274747_38274770del, NM_005955.2:c.*6045_*6068del (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.38274747_38274770del
DNA change (hg38) g.37809075_37809098del
Published as C1orf122(NM_001142726.1):c.139_*18del (p.(=))
ISCN -
DB-ID C1orf122_000003
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_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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTF1 NM_005955.2 ?/. - c.*6045_*6068del r.(=) p.(=)
YRDC NM_024640.3 ?/. - c.-911_-888del r.(?) p.(=)
C1orf122 NM_198446.2 ?/. - c.*2_*25del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.