Variant #0000253820 (NC_000007.13:g.91871519del, NC_000007.13(NM_194454.1):c.-2-61del (KRIT1))

Chromosome 7
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.91871519del
DNA change (hg38) g.92242205del
Published as KRIT1(NM_004912.4):c.-2-61delT
ISCN -
DB-ID KRIT1_000076
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 2018-01-15 20:58:59 +01:00 (CET)
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.-4405del r.(?) p.(=)
KRIT1 NM_194454.1 -/. - c.-2-61del r.(=) p.(=)


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