Variant #0000809513 (NC_000022.10:g.24720252C>T, NR_103546.1:n.2311C>T (SPECC1L-ADORA2A))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.24720252C>T
DNA change (hg38) -
Published as SPECC1L(NM_001145468.2):c.2003C>T (p.(Thr668Met)), SPECC1L(NM_015330.6):c.2003C>T (p.T668M)
ISCN -
DB-ID SPECC1L-ADORA2A_000007 See all 2 reported entries
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) 0.00043 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 2021-09-17 14:40:49 +02:00 (CEST)
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     
SPECC1L NM_015330.3 ?/. - c.2003C>T r.(?) p.(Thr668Met)
SPECC1L-ADORA2A NR_103546.1 ?/. - n.2311C>T r.(?) -


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