Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
-/ATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGC... Click the plus to show all of the alleles
Location

Chromosome 17: between 63488529 and 63488530 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 24 HGVS names - Hide

Variant allele ATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC
17:g.63488529_63488530insATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC
ENST00000582005.5:c.*226-105_*226-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000578839.5:c.*376-105_*376-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000584865.5:n.252-105_252-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000428043.5:c.2306-105_2306-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000290866.9:c.2306-105_2306-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000582761.1:c.74-105_74-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000579314.5:c.584-27_584-26insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000579204.1:c.*376-27_*376-26insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000290863.10:c.584-105_584-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000577647.2:c.584-105_584-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
ENST00000413513.7:c.584-105_584-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT

Variant allele G
17:g.63488529_63488530insG
ENST00000582005.5:c.*226-119_*226-118insG
ENST00000578839.5:c.*376-119_*376-118insG
ENST00000584865.5:n.252-119_252-118insG
ENST00000428043.5:c.2306-119_2306-118insG
ENST00000290866.9:c.2306-119_2306-118insG
ENST00000582761.1:c.74-119_74-118insG
ENST00000579314.5:c.584-41_584-40insG
ENST00000579204.1:c.*376-41_*376-40insG
ENST00000290863.10:c.584-119_584-118insG
ENST00000577647.2:c.584-119_584-118insG
ENST00000413513.7:c.584-119_584-118insG

About this variant

This variant overlaps 32 transcripts, 1 regulatory feature, is associated with 1 phenotype and is mentioned in 49 citations.

Variant displays