Variant #0000566317 (NC_000019.9:g.14046615C>T, NM_017721.4:c.*5407C>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.14046615C>T
DNA change (hg38) g.13935802C>T
Published as PODNL1(NM_001146254.1):c.428G>A (p.(Arg143Gln))
ISCN -
DB-ID CC2D1A_000037
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) 3.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D1A NM_017721.4 -?/. - c.*5407C>T r.(=) p.(=)
PODNL1 NM_024825.3 -?/. - c.434G>A r.(?) p.(Arg145Gln)
DCAF15 NM_138353.2 -?/. - c.-16710C>T r.(?) p.(=)


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