Variant #0000605109 (NC_000001.10:g.203143634G>A, NM_001276.2:c.*4939C>T (CHI3L1))

Chromosome 1
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.203143634G>A
DNA change (hg38) g.203174506G>A
Published as MYBPH(NM_004997.3):c.432C>T (p.R144=)
ISCN -
DB-ID CHI3L1_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) 5.0E-5 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHI3L1 NM_001276.2 -?/. - c.*4939C>T r.(=) p.(=)
MYBPH NM_004997.2 -?/. - c.432C>T r.(?) p.(Arg144=)


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