Variant #0000923851 (NC_000003.11:g.14487265C>T, NM_001080423.2:c.*47908G>A (GRIP2))

Chromosome 3
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.14487265C>T
DNA change (hg38) -
Published as SLC6A6(NM_001134367.3):c.581C>T (p.P194L)
ISCN -
DB-ID GRIP2_000002
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) 0.00108 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIP2 NM_001080423.2 -/. - c.*47908G>A r.(=) p.(=)
SLC6A6 NM_003043.3 -/. - c.270C>T r.(?) p.(Ser90=)


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