chr1:209806122:C>T Detail (hg19) (LAMB3)

Information

Genome

Assembly Position
hg19 chr1:209,806,122-209,806,122
hg38 chr1:209,632,777-209,632,777 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000228.2:c.629-1G>A
NM_001017402.1:c.629-1G>A
NM_001127641.1:c.629-1G>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 150310 OMIM
HGNC 6490 HGNC
Ensembl ENSG00000196878 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 2007-05-01 no assertion criteria provided Junctional epidermolysis bullosa, non-Herlitz type somatic Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.560 Adult junctional epidermolysis bullosa (disorder) NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000228.3(LAMB3):c.629-1G>A AND Junctional epidermolysis bullosa, non-Herlitz type ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs587776814 dbSNP
Genome
hg19
Position
chr1:209,806,122-209,806,122
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser