Variant #0000532990 (NC_000007.13:g.91874914C>A, NC_000007.13(NM_194454.1):c.-421+190G>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.91874914C>A
DNA change (hg38) g.92245600C>A
Published as KRIT1(NM_194456.1):c.-589-5G>T
ISCN -
DB-ID ANKIB1_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKIB1 NM_019004.1 -?/. - c.-1010C>A r.(?) p.(=)
KRIT1 NM_194454.1 -?/. - c.-421+190G>T r.(=) p.(=)


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