Variant #0000274313 (NC_000002.11:g.3691324C>T, NM_024027.4:c.432C>T (COLEC11))

Chromosome 2
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.3691324C>T
DNA change (hg38) g.3643734C>T
Published as COLEC11(NM_001255982.1):c.360C>T (p.(Ala120=)), COLEC11(NM_199235.2):c.423C>T (p.A141=), COLEC11(NM_199235.3):c.423C>T (p.A141=)
ISCN -
DB-ID COLEC11_000012 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) 0.00371 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COLEC11 NM_024027.4 -?/. - c.432C>T r.(?) p.(Ala144=)


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