Variant #0000991225 (NC_000001.10:g.38323234T>C, NM_005955.2:c.97A>G (MTF1))

Chromosome 1
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.38323234T>C
DNA change (hg38) -
Published as MTF1(NM_005955.2):c.97A>G (p.(Asn33Asp))
ISCN -
DB-ID INPP5B_000006
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 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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP5B NM_005540.2 -?/. - c.*4753A>G r.(=) p.(=)
MTF1 NM_005955.2 -?/. - c.97A>G r.(?) p.(Asn33Asp)


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