Variant #0000525370 (NC_000005.9:g.178419280_178419281insGCAAGGTCTG, NC_000005.9(NM_000843.3):c.505-196_505-195insAGACCTTGCC (GRM6))

Chromosome 5
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.178419280_178419281insGCAAGGTCTG
DNA change (hg38) g.178992279_178992280insGCAAGGTCTG
Published as GRM6(NM_000843.4):c.505-197_505-196insCAGACCTTGC
ISCN -
DB-ID GRM6_000073
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM6 NM_000843.3 -/. - c.505-196_505-195insAGACCTTGCC r.(=) p.(=)


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