Variant #0000612037 (NC_000009.11:g.140063759_140063760insAT, NM_007327.3:c.*1780_*1781insAT (GRIN1))

Chromosome 9
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.140063759_140063760insAT
DNA change (hg38) g.137169307_137169308insAT
Published as LRRC26(NM_001013653.2):c.636_637insAT (p.(Cys213IlefsTer26))
ISCN -
DB-ID GRIN1_000052
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) 0.0003 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 13:06:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC26 NM_001013653.2 ?/. - c.636_637insAT r.(?) p.(Cys213IlefsTer26)
GRIN1 NM_007327.3 ?/. - c.*1780_*1781insAT r.(=) p.(=)
TMEM210 XM_003846333.2 ?/. - c.*1667_*1668insAT r.(=) p.(=)


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