Variant #0000532839 (NC_000007.13:g.86817539G>T, NM_021145.3:c.1333G>T (DMTF1))

Chromosome 7
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.86817539G>T
DNA change (hg38) g.87188223G>T
Published as DMTF1(NM_001142327.1):c.1333G>T (p.(Ala445Ser))
ISCN -
DB-ID DMTF1_000002
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) 0.00019 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.1333G>T r.(?) p.(Ala445Ser)
TMEM243 NM_024315.2 ?/. - c.*8413C>A r.(=) p.(=)


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