Variant #0000272276 (NC_000011.9:g.73796878T>C, NM_015531.4:c.3695A>G (C2CD3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73796878T>C
DNA change (hg38) g.74085833T>C
Published as C2CD3(NM_001286577.1):c.3695A>G (p.N1232S), C2CD3(NM_001286577.2):c.3695A>G (p.(Asn1232Ser))
ISCN -
DB-ID C2CD3_000004 See all 4 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) 0.00708 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2CD3 NM_015531.4 -/. - c.3695A>G r.(?) p.(Asn1232Ser)


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