Variant #0000536419 (NC_000009.11:g.131389060_131389061insAA, NC_000009.11(NM_001130438.2):c.6576+94_6576+95insAA (SPTAN1))

Chromosome 9
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.131389060_131389061insAA
DNA change (hg38) g.128626781_128626782insAA
Published as SPTAN1(NM_001130438.2):c.6576+94_6576+95insAA
ISCN -
DB-ID WDR34_000017
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
SPTAN1 NM_001130438.2 -/. - c.6576+94_6576+95insAA r.(=) p.(=)
WDR34 NM_052844.3 -/. - c.*6962_*6963insTT r.(=) p.(=)


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