Variant #0000992832 (NC_000002.11:g.36775698G>T, NM_016441.2:c.2965G>T (CRIM1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36775698G>T
DNA change (hg38) -
Published as CRIM1(NM_016441.2):c.2965G>T (p.(Val989Leu))
ISCN -
DB-ID CRIM1_000025
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FEZ2 NM_001042548.1 ?/. - c.*4608C>A r.(=) p.(=)
CRIM1 NM_016441.2 ?/. - c.2965G>T r.(?) p.(Val989Leu)


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