Variant #0000613709 (NC_000011.9:g.73879623G>A, NM_015531.4:c.91C>T (C2CD3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73879623G>A
DNA change (hg38) g.74168578G>A
Published as C2CD3(NM_001286577.2):c.91C>T (p.P31S)
ISCN -
DB-ID C2CD3_000051
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +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     
C2CD3 NM_015531.4 +?/. - c.91C>T r.(?) p.(Pro31Ser)
PPME1 NM_016147.1 +?/. - c.-2844G>A r.(?) p.(=)


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