Variant #0000538279 (NC_000009.11:g.43626510A>C, NM_001145196.1:c.2177T>G (SPATA31A6))

Chromosome 9
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.43626510A>C
DNA change (hg38) g.42187879T>G
Published as SPATA31A6(NM_001145196.1):c.2177T>G (p.L726R, p.(Leu726Arg))
ISCN -
DB-ID SPATA31A6_000006 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) Retrieve
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPATA31A6 NM_001145196.1 ?/. - c.2177T>G r.(?) p.(Leu726Arg)


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