Variant #0000655267 (NC_000005.9:g.127800637_127800640del, NC_000005.9(NM_001999.3):c.629-18_629-15del (FBN2))

Chromosome 5
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.127800637_127800640del
DNA change (hg38) g.128464944_128464947del
Published as FBN2(NM_001999.4):c.629-18_629-15delTCTT
ISCN -
DB-ID FBN2_000252
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBN2 NM_001999.3 -?/. - c.629-18_629-15del r.(=) p.(=)


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