chr17:29527439:G>T Detail (hg19) (NF1)

Information

Genome

Assembly Position
hg19 chr17:29,527,439-29,527,439
hg38 chr17:31,200,421-31,200,421 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000267.3:c.889-1G>T
NM_001128147.2:c.889-1G>T
NM_001042492.2:c.889-1G>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 613113 OMIM
HGNC 7765 HGNC
Ensembl ENSG00000196712 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic 2014-02-21 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
Pathogenic 2023-04-06 criteria provided, single submitter Neurofibromatosis, type 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.120 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_001042492.3(NF1):c.889-1G>T AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_001042492.3(NF1):c.889-1G>T AND Neurofibromatosis, type 1 ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs587781517 dbSNP
Genome
hg19
Position
chr17:29,527,439-29,527,439
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Genome browser