Variant #0000681308 (NC_000019.9:g.14038794C>T, NM_017721.4:c.2405C>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.14038794C>T
DNA change (hg38) -
Published as CC2D1A(NM_017721.4):c.2405C>T (p.(Thr802Met))
ISCN -
DB-ID CC2D1A_000041
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.2405C>T r.(?) p.(Thr802Met)
PODNL1 NM_024825.3 -?/. - c.*4724G>A r.(=) p.(=)
DCAF15 NM_138353.2 -?/. - c.-24531C>T r.(?) p.(=)


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