Variant #0000557080 (NC_000016.9:g.2090217dup, NM_002528.5:c.733dup (NTHL1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2090217dup
DNA change (hg38) g.2040216dup
Published as NTHL1(NM_002528.7):c.709dupA (p.I237Nfs*28)
ISCN -
DB-ID NTHL1_000016
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-07 14:06:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A3R2 NM_001130012.2 +?/. - c.*2232dup r.(?) p.(=)
NTHL1 NM_002528.5 +?/. - c.733dup r.(?) p.(Ile245AsnfsTer28)


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