Variant #0000861712 (NC_000009.11:g.4625321G>A, NM_004170.5:c.*39763G>A (SLC1A1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4625321G>A
DNA change (hg38) -
Published as SPATA6L(NM_001353491.1):c.300+6C>T
ISCN -
DB-ID PPAPDC2_000004
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 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 15:51:19 +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     
SPATA6L NM_001039395.3 -?/. - c.495+6C>T r.(=) p.(=)
SLC1A1 NM_004170.5 -?/. - c.*39763G>A r.(=) p.(=)
PPAPDC2 NM_203453.3 -?/. - c.-37055G>A r.(?) p.(=)


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