Variant #0000308765 (NC_000014.8:g.88852166G>A, NM_018418.4:c.4G>A (SPATA7))

Chromosome 14
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.88852166G>A
DNA change (hg38) g.88385822G>A
Published as SPATA7(NM_018418.4):c.4G>A (p.D2N), SPATA7(NM_018418.5):c.4G>A (p.D2N)
ISCN -
DB-ID SPATA7_000006 See all 5 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) 0.33025 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPATA7 NM_018418.4 -/. - c.4G>A r.(?) p.(Asp2Asn)


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