Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 14:94849228 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900180

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 29 HGVS names - click the plus to show

14:g.94849228A>T
ENST00000556955.1:c.347T>A
ENSP00000451098.1:p.Ile116Asn
ENST00000448921.1:c.347T>A
ENSP00000416066.1:p.Ile116Asn
ENST00000449399.3:c.347T>A
ENSP00000416354.3:p.Ile116Asn
ENST00000554720.1:c.89T>A
ENSP00000450561.1:p.Ile30Asn
ENST00000355814.4:c.347T>A
ENSP00000348068.4:p.Ile116Asn
ENST00000404814.4:c.347T>A
ENSP00000385960.4:p.Ile116Asn
ENST00000557492.1:c.347T>A
ENSP00000452452.1:p.Ile116Asn
ENST00000393088.4:c.347T>A
ENSP00000376803.4:p.Ile116Asn
ENST00000393087.4:c.347T>A
ENSP00000376802.4:p.Ile116Asn
ENST00000437397.1:c.347T>A
ENSP00000408474.1:p.Ile116Asn
ENST00000402629.1:c.347T>A
ENSP00000386094.1:p.Ile116Asn
ENST00000489769.1:c.347T>A
ENSP00000451525.1:p.Ile116Asn
ENST00000440909.1:c.347T>A
ENSP00000390299.1:p.Ile116Asn
ENST00000556091.1:c.347T>A
ENSP00000452169.1:p.Ile116Asn

Variation displays