Variant #0000266515 (NC_000019.9:g.14038731G>T, NM_017721.4:c.2342G>T (CC2D1A))

Chromosome 19
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.14038731G>T
DNA change (hg38) g.13927918G>T
Published as CC2D1A(NM_017721.5):c.2342G>T (p.G781V)
ISCN -
DB-ID CC2D1A_000018
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) 0.00121 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D1A NM_017721.4 -?/. - c.2342G>T r.(?) p.(Gly781Val)
PODNL1 NM_024825.3 -?/. - c.*4787C>A r.(=) p.(=)
DCAF15 NM_138353.2 -?/. - c.-24594G>T r.(?) p.(=)


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