Variant #0000613504 (NC_000011.9:g.63974815C>T, NC_000011.9(NM_031471.5):c.-14-8C>T (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.63974815C>T
DNA change (hg38) g.64207343C>T
Published as FERMT3(NM_178443.2):c.-14-8C>T
ISCN -
DB-ID FERMT3_000020
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*3217C>T r.(=) p.(=)
FERMT3 NM_031471.5 ?/. - c.-14-8C>T r.(=) p.(=)
TRPT1 NM_031472.3 ?/. - c.*16533G>A r.(=) p.(=)


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