Variant #0000288874 (NC_000013.10:g.113980125C>A, NM_024719.2:c.772G>T (GRTP1))

Chromosome 13
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.113980125C>A
DNA change (hg38) g.113325810C>A
Published as GRTP1(NM_001286732.1):c.772G>T (p.G258C)
ISCN -
DB-ID GRTP1_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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMP1 NM_005561.3 ?/. - c.*3389C>A r.(=) p.(=)
GRTP1 NM_024719.2 ?/. - c.772G>T r.(?) p.(Gly258Cys)


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