Variant #0000608371 (NC_000003.11:g.14508105G>A, NM_001080423.2:c.*27068C>T (GRIP2))

Chromosome 3
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.14508105G>A
DNA change (hg38) g.14466597G>A
Published as SLC6A6(NM_003043.6):c.814G>A (p.E272K)
ISCN -
DB-ID GRIP2_000001
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) 2.0E-5 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIP2 NM_001080423.2 ?/. - c.*27068C>T r.(=) p.(=)
SLC6A6 NM_003043.3 ?/. - c.814G>A r.(?) p.(Ala272Thr)


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