Variant #0000279092 (NC_000002.11:g.128397728G>C, NC_000002.11(NM_001136037.2):c.869-8C>G (LIMS2))

Chromosome 2
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.128397728G>C
DNA change (hg38) g.127640153G>C
Published as LIMS2(NM_001161404.2):c.788-8C>G
ISCN -
DB-ID LIMS2_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) 0.01389 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO7B NM_001080527.1 -/. - c.*2736G>C r.(=) p.(=)
LIMS2 NM_001136037.2 -/. - c.869-8C>G r.(=) p.(=)
GPR17 NM_001161415.1 -/. - c.-6322G>C r.(?) p.(=)


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