Variant #0000862615 (NC_000011.9:g.63974995C>G, NM_031471.5:c.159C>G (FERMT3))

Chromosome 11
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.63974995C>G
DNA change (hg38) -
Published as FERMT3(NM_031471.5):c.159C>G (p.(Ile53Met)), FERMT3(NM_031471.6):c.159C>G (p.I53M), FERMT3(NM_178443.2):c.159C>G (p.I53M)
ISCN -
DB-ID FERMT3_000014 See all 3 reported entries
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) 0.00193 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STIP1 NM_006819.2 ?/. - c.*3397C>G r.(=) p.(=)
FERMT3 NM_031471.5 ?/. - c.159C>G r.(?) p.(Ile53Met)
TRPT1 NM_031472.3 ?/. - c.*16353G>C r.(=) p.(=)


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