Variant #0000503889 (NC_000001.10:g.158637728T>C, NM_003126.2:c.1958A>G (SPTA1))

Chromosome 1
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.158637728T>C
DNA change (hg38) g.158667938T>C
Published as SPTA1(NM_003126.2):c.1958A>G (p.(Tyr653Cys)), SPTA1(NM_003126.3):c.1958A>G (p.Y653C)
ISCN -
DB-ID SPTA1_000093 See all 3 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) 0.00817 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
SPTA1 NM_003126.2 -?/. - c.1958A>G r.(?) p.(Tyr653Cys)


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