chr18:57554259:C>T Detail (hg38) (FECH)

Information

Genome

Assembly Position
hg19 chr18:55,221,491-55,221,491 View the variant detail on this assembly version.
hg38 chr18:57,554,259-57,554,259

HGVS

Type Transcript Protein
RefSeq NM_000140.3:c.1077+1G>A
NM_001012515.2:c.861+1G>A
Ensemble ENST00000262093.11:c.1077+1G>A
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 612386 OMIM
HGNC 3647 HGNC
Ensembl ENSG00000066926 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 1993-05-01 no assertion criteria provided Protoporphyria, erythropoietic, 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.609 erythropoietic protoporphyria NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000140.5(FECH):c.1077+1G>A AND Protoporphyria, erythropoietic, 1 ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs786205245 dbSNP
Genome
hg38
Position
chr18:57,554,259-57,554,259
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser