Variant #0000532841 (NC_000007.13:g.86823175T>C, NM_021145.3:c.1785T>C (DMTF1))

Chromosome 7
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.86823175T>C
DNA change (hg38) g.87193859T>C
Published as DMTF1(NM_021145.3):c.1785T>C (p.I595=)
ISCN -
DB-ID DMTF1_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 10:17:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMTF1 NM_021145.3 -?/. - c.1785T>C r.(?) p.(Ile595=)
TMEM243 NM_024315.2 -?/. - c.*2777A>G r.(=) p.(=)


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