Variant #0000866746 (NC_000022.10:g.24730587C>T, NC_000022.10(NR_103546.1):n.2868+46C>T (SPECC1L-ADORA2A))

Chromosome 22
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.24730587C>T
DNA change (hg38) -
Published as SPECC1L(NM_015330.4):c.2560+46C>T
ISCN -
DB-ID SPECC1L_000016
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) 0.53918 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPECC1L NM_015330.3 -/. - c.2560+46C>T r.(=) p.(=)
SPECC1L-ADORA2A NR_103546.1 -/. - n.2868+46C>T r.(?) -


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