Variant #0000924440 (NC_000006.11:g.146480773_146480778del, NC_000006.11(NM_001278064.1):c.950+40_950+45del (GRM1))

Chromosome 6
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.146480773_146480778del
DNA change (hg38) -
Published as GRM1(NM_001278064.1):c.950+8_950+13del (p.(=)), GRM1(NM_001278064.2):c.950+40_950+45delTCTCTC
ISCN -
DB-ID GRM1_000043 See all 2 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) 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM1 NM_000838.3 -/. - c.950+40_950+45del r.(=) p.(=)
GRM1 NM_001278064.1 -/. - c.950+40_950+45del r.(=) p.(=)


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