Variant #0000509635 (NC_000002.11:g.152582014T>C, NM_001271208.1:c.355A>G (NEB))

Chromosome 2
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.152582014T>C
DNA change (hg38) g.151725500T>C
Published as NEB(NM_001164507.1):c.355A>G (p.(Thr119Ala)), NEB(NM_001271208.1):c.355A>G (p.T119A)
ISCN -
DB-ID NEB_000721 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) 0.00029 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
NEB NM_001271208.1 ?/. - c.355A>G - r.(?) p.(Thr119Ala)


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