Variant #0000888018 (NC_000007.13:g.91875208C>A, NM_194454.1:c.-525G>T (KRIT1))

Chromosome 7
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.91875208C>A
DNA change (hg38) -
Published as KRIT1(NM_194456.1):c.-590+12G>T
ISCN -
DB-ID ANKIB1_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKIB1 NM_019004.1 -?/. - c.-716C>A r.(?) p.(=)
KRIT1 NM_194454.1 -?/. - c.-525G>T r.(?) p.(=)


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