Variant #0000562284 (NC_000017.10:g.4875559C>T, NM_004890.2:c.-4460G>A (SPAG7))

Chromosome 17
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.4875559C>T
DNA change (hg38) g.4972264C>T
Published as CAMTA2(NM_001171167.1):c.2845G>A (p.A949T)
ISCN -
DB-ID CAMTA2_000001
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) 2.0E-5 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 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     
SPAG7 NM_004890.2 ?/. - c.-4460G>A r.(?) p.(=)
CAMTA2 NM_015099.3 ?/. - c.2776G>A r.(?) p.(Ala926Thr)


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