Variant #0000848721 (NC_000001.10:g.38019657G>T, NM_024700.3:c.174C>A (SNIP1))

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.38019657G>T
DNA change (hg38) -
Published as SNIP1(NM_024700.3):c.174C>A (p.S58R)
ISCN -
DB-ID DNALI1_000003
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) 0.00075 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 15:40:45 +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     
DNALI1 NM_003462.3 -?/. - c.-2873G>T r.(?) p.(=)
GNL2 NM_013285.2 -?/. - c.*12799C>A r.(=) p.(=)
SNIP1 NM_024700.3 -?/. - c.174C>A r.(?) p.(Ser58Arg)


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