Variant #0000276547 (NC_000005.9:g.153381917_153381932del, NM_018691.2:c.1136_1151del (FAM114A2))

Chromosome 5
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.153381917_153381932del
DNA change (hg38) g.154002357_154002372del
Published as FAM114A2(NM_018691.4):c.1136_1151delTCCGGAGCCTGGCTGA (p.I379Nfs*2)
ISCN -
DB-ID FAM114A2_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-18 09:06:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM114A2 NM_018691.2 ?/. - c.1136_1151del r.(?) p.(Ile379AsnfsTer2)


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