Variant #0000691912 (NC_000015.9:g.90774393G>C, NM_006384.3:c.399C>G (CIB1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.90774393G>C
DNA change (hg38) -
Published as CIB1(NM_001277764.1):c.519C>G (p.N173K)
ISCN -
DB-ID CIB1_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDPGP1 NM_001013657.2 ?/. - c.-3273G>C r.(?) p.(=)
TTLL13 NM_001029964.2 ?/. - c.-18659G>C r.(?) p.(=)
NGRN NM_001033088.1 ?/. - c.-34552G>C r.(?) p.(=)
CIB1 NM_006384.3 ?/. - c.399C>G r.(?) p.(Asn133Lys)
SEMA4B NM_198925.2 ?/. - c.*2518G>C r.(=) p.(=)


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