Variant #0001005059 (NC_000019.9:g.51169534G>C, NM_016148.2:c.5683C>G (SHANK1))

Chromosome 19
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.51169534G>C
DNA change (hg38) -
Published as SHANK1(NM_016148.2):c.5683C>G (p.(Arg1895Gly))
ISCN -
DB-ID C19orf81_000025
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) 1.0E-5 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 2024-08-28 13:16:32 +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     
C19orf81 NM_001195076.1 -?/. - c.*7135G>C r.(=) p.(=)
SHANK1 NM_016148.2 -?/. - c.5683C>G r.(?) p.(Arg1895Gly)


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