chr17:29527496:GC>AA Detail (hg19) (NF1)

Information

Genome

Assembly Position
hg19 chr17:29,527,496-29,527,497
hg38 chr17:31,200,478-31,200,479 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_001128147.2:c.945_946delinsAA NP_001121619.1:p.Leu316Met
NM_000267.3:c.945_946delinsAA NP_000258.1:p.Leu316Met
NM_001042492.2:c.945_946delinsAA NP_001035957.1:p.Leu316Met
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance 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
Pathogenic 2003-11-01 no assertion criteria provided Neurofibromatosis, type 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.482 neurofibromatosis-Noonan syndrome NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_001042492.3(NF1):c.945_946delinsAA (p.Leu316Met) AND Neurofibromatosis, type 1 ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs267606609 dbSNP
Genome
hg19
Position
chr17:29,527,496-29,527,497
Variant Type
snv
Reference Allele
GC
Alternative Allele
AA
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