Variant #0000290541 (NC_000007.13:g.91871373C>T, NM_194454.1:c.77G>A (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.91871373C>T
DNA change (hg38) g.92242059C>T
Published as KRIT1(NM_001013406.1):c.77G>A (p.(Arg26Gln)), KRIT1(NM_004912.4):c.77G>A (p.R26Q), KRIT1(NM_194455.1):c.77G>A (p.R26Q)
ISCN -
DB-ID KRIT1_000075 See all 3 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) 0.00104 View details
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 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKIB1 NM_019004.1 -/. - c.-4551C>T r.(?) p.(=)
KRIT1 NM_194454.1 -/. - c.77G>A r.(?) p.(Arg26Gln)


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