Variant #0000544807 (NC_000011.9:g.63978123A>G, NM_031471.5:c.201A>G (FERMT3))

Chromosome 11
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.63978123A>G
DNA change (hg38) g.64210651A>G
Published as FERMT3(NM_178443.2):c.201A>G (p.E67=)
ISCN -
DB-ID FERMT3_000015
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_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 2020-06-30 17:19:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FERMT3 NM_031471.5 -?/. - c.201A>G r.(?) p.(Glu67=)
TRPT1 NM_031472.3 -?/. - c.*13225T>C r.(=) p.(=)


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