Variant #0000926088 (NC_000015.9:g.90775443G>A, NC_000015.9(NM_006384.3):c.195+8C>T (CIB1))

Chromosome 15
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.90775443G>A
DNA change (hg38) -
Published as CIB1(NM_001277764.1):c.315+8C>T, CIB1(NM_006384.4):c.195+8C>T
ISCN -
DB-ID CIB1_000008 See all 2 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) 0.00078 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
GDPGP1 NM_001013657.2 -?/. - c.-2223G>A r.(?) p.(=)
TTLL13 NM_001029964.2 -?/. - c.-17609G>A r.(?) p.(=)
NGRN NM_001033088.1 -?/. - c.-33502G>A r.(?) p.(=)
CIB1 NM_006384.3 -?/. - c.195+8C>T r.(=) p.(=)
SEMA4B NM_198925.2 -?/. - c.*3568G>A r.(=) p.(=)


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