http://identifiers.org/hco/11/GRCh38#134412362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26644952-A-C

134412719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26644597-G-A

134412814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26644469-G-A

134412945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26644347-C-T

134413320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643956-A-G

134413321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643955-G-C

134413394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643891-G-A

134413952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643666-C-T

134414143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643457-C-T

134414174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643423-G-T

134414271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643266-G-A

134414326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26643213-C-T

134414581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26642971-A-G

134414581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26642971-A-T

134414683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26642878-C-T

134415247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26642347-G-A

http://identifiers.org/hco/11/GRCh38#134415305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26642288-C-A

134415492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26642116-T-G

134415665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641939-G-C

134415799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641819-T-C

134415815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641803-G-A

134415815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641803-G-T

134415895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641765-A-G

134416017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641656-G-A

134416334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641371-C-T

134416543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641177-T-A

134416543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26641177-T-G

134416798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26640922-G-A

134417685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639912-C-G

134417685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639912-C-T

134417798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639765-G-A

134417798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639765-G-T

134417801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639762-C-T

134417838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639725-T-C

134418140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639439-C-G

134418199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26639378-C-T

134418871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638729-G-T

134419007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638612-C-T

134419068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638551-G-T

http://identifiers.org/hco/11/GRCh38#134419153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26638453-C-A

134419153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638453-C-G

134419153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638453-C-T

134419157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638449-G-T

134419312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638286-T-C

134419576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26638034-C-T

134419768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26637870-C-T

134420594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26637172-A-G

134420736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26637092-A-T

134421082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26636791-C-T

134421672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26636226-T-C

134421759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26636147-T-G

134421844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26636066-C-T

134422101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26635703-C-T

134422275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26635529-G-T

134422396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26635417-C-T

134422614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26635187-G-T

134422615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26635186-T-C

134422782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26635005-C-T

134423004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634798-G-A

134423018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634784-T-C

134423059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634744-A-T

134423188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634632-G-A

134423238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634591-C-T

134423327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634524-T-C

http://identifiers.org/hco/11/GRCh38#134423392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26634489-C-A

http://identifiers.org/hco/11/GRCh38#134423648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26634259-A-C

134423648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26634259-A-G

http://identifiers.org/hco/11/GRCh38#134425378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26633817-C-A

134425423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633766-T-C

134425425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633764-G-C

134425451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633735-C-T

134425582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633604-T-G

134425920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633293-C-G

134425941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633272-G-T

134426120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26633113-T-G

http://identifiers.org/hco/11/GRCh38#134426469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26632763-A-C

134426469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26632763-A-G

134426878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26632377-G-A

134426934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26632321-C-G

134427039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26632224-T-C

134427044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26632219-A-T

134427262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26632015-C-T

134427407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26631735-A-G

134427488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26631646-C-T

134427594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26631499-C-T

134428045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26631087-A-G

134428096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26631036-G-A

134428305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26630869-T-C

134428940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26630271-T-A

134429086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26630127-A-G

134429104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26630109-C-T

134429200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26630013-G-A

134429378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629835-A-G

134429430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629783-G-A

134429546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629678-G-T

134429700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629538-A-T

http://identifiers.org/hco/11/GRCh38#134429812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26629438-C-A

134430005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629236-T-A

134430005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629236-T-C

134430106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629146-T-C

134430107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629145-C-T

134430148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629099-G-A

134430174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629073-G-A

134430174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629073-G-C

134430242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629021-G-A

134430242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629021-G-T

134430263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629000-C-G

134430263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26629000-C-T

134430523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26628818-A-G

134430818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26628184-C-T

134431091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26627457-A-T

134431759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26627004-G-T

134431769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26626994-A-G

134433222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26624220-T-G

134433328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26624118-T-C

134433441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26624035-C-T

134433446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26624030-G-A

134433758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26623756-C-T

134434293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26623237-G-A

http://identifiers.org/hco/11/GRCh38#134434464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26623053-C-A

134434464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26623053-C-T

134434638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622894-G-A

134435460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622615-T-C

134435540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622532-G-C

134435540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622532-G-T

134435650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622405-C-T

134436005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622128-C-G

134436005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26622128-C-T

134436293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621874-A-G

134436293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621874-A-T

http://identifiers.org/hco/11/GRCh38#134436383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26621703-C-A

134436383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621703-C-T

134436389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621697-G-C

134436389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621697-G-T

134436405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621683-G-A

134436405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621683-G-T

134436433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26621655-G-T

134436524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621560-G-T

134436553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621533-G-A

134436553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621533-G-T

134436570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621516-A-G

134436576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621510-T-C

134436584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621501-T-C

http://identifiers.org/hco/11/GRCh38#134436593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26621492-C-A

134436593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621492-C-T

134436616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26621468-A-G

http://identifiers.org/hco/11/GRCh38#134436687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26621395-C-A

http://identifiers.org/hco/11/GRCh38#134436695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26621387-C-A

134437023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620703-G-A

134437088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620638-C-G

134437279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620516-C-T

134437352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620444-A-G

134437369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620418-C-T

134437376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620412-T-C

134437440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620331-G-A

134437478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620276-T-C

134437489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620265-T-C

134437514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620240-C-T

134437546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26620208-A-G

134438380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26619923-G-C

134438390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26619913-G-A

134438416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26619866-C-T

134438424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26619858-C-T

134438465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26619818-C-G

134438465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26619818-C-T

134438834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26619452-C-T

134439025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26612125-G-A

134439100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26612048-G-A

134439411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26611726-G-A

134439423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26611716-T-C

134439543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26611608-G-A

134439570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26611579-G-C

http://identifiers.org/hco/11/GRCh38#134441162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26611085-C-A

134441164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26611083-C-T

134441280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26610957-G-A

134441280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26610957-G-T

134441423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26610809-C-T

134441625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26610674-T-C

134441696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26610622-T-C

134442225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26610042-C-T

134442392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26609867-G-A

134442517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26609755-T-G

134442543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26609730-C-T

134442613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26609665-A-G

134442638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26609638-C-T

134442665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26609616-A-G

134442804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26607013-C-T

http://identifiers.org/hco/11/GRCh38#134442839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26606978-C-A

134442839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26606978-C-T

134443410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26606476-G-A

134443410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26606476-G-T

134443467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26606416-C-T

134444040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26605883-C-T

134444158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26605770-C-T

134450049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601427-T-A

134450258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601216-A-G

134452015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598869-G-A

134452189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598739-G-A

134452189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598739-G-T

134452337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598612-T-A

http://identifiers.org/hco/11/GRCh38#134452402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26598539-C-A

134452410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598531-T-C

134452416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598526-C-T

134452490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598452-G-A

134452608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598338-G-T

134453177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26597810-C-T

134453324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26597660-T-C

134453456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26597553-T-G

134454079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26596967-T-A

134454157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26596923-G-A

134454159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26596921-A-G

134456950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26593098-G-A

134456950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26593098-G-T

134456960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26593090-G-T

134457136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592900-A-T

134457930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592356-T-G

134457993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592292-G-A

134457994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592291-T-A

134458013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592272-G-C

134458022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592263-C-G

134458022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26592263-C-T

134459579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26590422-G-A

134459721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26590310-T-C

134459787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26590240-G-A

134459927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26590088-C-G

134460125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589895-C-G

134460125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589895-C-T

134460128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589892-G-A

134460130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589890-T-C

134460315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589708-C-G

134460377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589593-C-T

http://identifiers.org/hco/11/GRCh38#134460681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26589082-C-A

134460681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26589082-C-G

http://identifiers.org/hco/11/GRCh38#134460781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26588985-A-C

134460781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26588985-A-G

134463797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26584276-C-T

134463834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26584239-G-A

134464073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26584019-A-T

134464257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583613-G-A

134464552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583349-C-T

134464564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583337-G-C

134464587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583314-C-G

134464588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583313-C-T

http://identifiers.org/hco/11/GRCh38#134464655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26583248-C-A

134464655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583248-C-T

134464874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582923-T-A

134464992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582823-G-A

134465066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582767-C-G

134465130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582746-A-G

134465133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582743-A-G

134465241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582645-G-A

134465241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582645-G-C

134465341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582548-G-A

134465576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582307-T-C

134465842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582032-C-G

134465853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26582021-T-C

134466086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26581795-T-A

134466097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26581784-C-T

134466269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26581636-T-C

134466706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580230-A-G

http://identifiers.org/hco/11/GRCh38#134466711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26580225-C-A

134466711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580225-C-G

http://identifiers.org/hco/11/GRCh38#134466911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26580045-C-A

http://identifiers.org/hco/11/GRCh38#134466917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26580042-C-A

134466917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580042-C-G

134466917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580042-C-T

134466925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580034-T-A

134466925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580034-T-C

134466968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26580004-T-C

134468153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26579452-A-G

134468286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26579318-T-C

134468289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26579315-G-A

http://identifiers.org/hco/11/GRCh38#134468980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26578772-C-A

134469423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578355-T-C

http://identifiers.org/hco/11/GRCh38#134469615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#26578169-C-A

134469625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26578159-A-G

134469645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26578148-A-G

134469655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26578138-G-A

134469655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26578138-G-C

134469750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26578027-T-C

134469821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26577956-T-C

134469821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26577956-T-G

134469966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26577828-G-T

134470031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26577772-C-T

134470083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26577709-C-T

134470115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26577678-G-T

134470991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26576128-G-T

134471024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26576102-A-T

134471272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575891-C-T

134471480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575683-G-A

134471484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575679-T-C

134471618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575577-C-T

http://identifiers.org/hco/11/GRCh38#134471737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26575471-A-C

134472049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575197-A-G

134472058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575188-A-G

134472058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575188-A-T

134472564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574619-T-A

134472564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574619-T-C

134472689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574521-G-C

134472764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574444-G-A

134472764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574444-G-C

134473413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573931-G-C

134473853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573619-G-A

134473853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573619-G-T

134473896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573583-A-G

134473983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573498-G-A

http://identifiers.org/hco/11/GRCh38#134474001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26573480-C-A

134474208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26571374-C-G

134474233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26571351-G-A

134474259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26571310-C-T

134474529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26571014-A-G

134474633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26570920-G-A

134474739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26570810-G-A

134474739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26570810-G-T

134474765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26570783-C-T

134474773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26570776-G-A

134474792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26570759-C-T

134477508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569443-C-T

134477683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569291-A-G

134477758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569230-A-T

134477762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569226-T-C

134477790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569195-C-T

134477796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569189-T-C

134477846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569139-C-T

134477958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569048-G-C

134477988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26569018-C-G

134478023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568984-T-G

134478057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568969-G-A

134478057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568969-G-C

134478061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568963-C-T

134478102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568922-C-T

134478123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568904-T-C

134478134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568893-T-A

134478151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568880-T-C

134478151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568880-T-G

134478298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568759-A-G

134478298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568759-A-T

134478305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568752-T-C

134478352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568694-C-T

134478403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568651-C-T

http://identifiers.org/hco/11/GRCh38#134478496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26568551-C-A

134478496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568551-C-G

134478496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568551-C-T

http://identifiers.org/hco/11/GRCh38#134478554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26568483-C-A

134478554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568483-C-T

134478559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568478-G-A

134478697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568039-C-T

134478769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567968-G-A

http://identifiers.org/hco/11/GRCh38#134478778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26567959-A-C

134478907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567777-A-G

134478926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567758-T-C

134478979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567706-T-C

134479023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567653-T-C

134479209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567413-G-A

134479253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567369-G-T

134479274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567348-G-T

134479289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26567334-G-T

http://identifiers.org/hco/11/GRCh38#134479305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26567318-C-A

134479305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26567318-C-T

134479320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26567290-G-A

134479320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26567290-G-T

134479351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26567037-G-A

134479351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26567037-G-T

134479395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566994-A-G

http://identifiers.org/hco/11/GRCh38#134479460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26566930-C-A

134479530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566855-C-T

134479545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566840-T-G

134479546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566839-T-C

http://identifiers.org/hco/11/GRCh38#134479615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26566778-C-A

134479615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566778-C-T

http://identifiers.org/hco/11/GRCh38#134479644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26566745-C-A

134479736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566653-T-A

134479834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566561-A-G

134479897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566497-G-A

134479897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566497-G-T

http://identifiers.org/hco/11/GRCh38#134480026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26566412-C-A

134480026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566412-C-T

134480052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566385-T-C

134480053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566384-G-A

134480053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566384-G-T

134480072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566371-A-G

134480078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566363-T-C

http://identifiers.org/hco/11/GRCh38#134480154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26566289-C-A

134480154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566289-C-T

134480228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566194-C-G

134480228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566194-C-T

134480313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566111-C-T

http://identifiers.org/hco/11/GRCh38#134480374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26566064-C-A

134480374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566064-C-T

134480389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566049-C-T

134480497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26566000-T-C

134480499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565998-G-A

134480511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565986-A-G

134480594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565909-C-T

134480603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565903-C-T

http://identifiers.org/hco/11/GRCh38#134480660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26565845-C-A

134480660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565845-C-T

134480701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565803-G-T

134480724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565781-G-A

134480741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565767-A-G

134480758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565750-A-G

134480765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565743-G-A

134480765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565743-G-T

134480817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26565065-T-C

134480843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 26565039-A-G

134481049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564861-T-C

134481071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564841-A-G

134481115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564807-G-T

134481207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564713-C-T

134481298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564630-G-A

134481622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564319-C-G

http://identifiers.org/hco/11/GRCh38#134481848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26564116-A-C

134481999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563968-C-T

134482035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563934-G-A

134482298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563723-C-T

134482339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563701-G-A

134482390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563672-T-C

134482391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563671-G-A

134482391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563671-G-T

134482413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563652-G-T

134482562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563502-G-A

134482677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26563398-A-G

134482719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26563356-A-G

134482874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563194-G-T

134483040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563037-C-T

134483201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562920-A-T

134483326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562810-G-A

134483460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562688-G-A

134483615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562623-T-G

134483739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562580-G-A

134483842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562478-A-G

134484223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562242-G-A

134484397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562075-T-C

134484476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562001-G-A

134484755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26561729-C-G

134484811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26561673-T-C

134488614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560165-T-G

134488766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560020-T-C

134488835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559936-G-C

134488835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559936-G-T

134488940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559824-C-T

134488968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559804-T-C

134488981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559793-G-C

134488982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559792-A-G

134489140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559682-C-T

134489145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559673-G-A

134489145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559673-G-C

http://identifiers.org/hco/11/GRCh38#134489239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26559536-C-A

134489241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559534-C-G

134489241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559534-C-T

134489305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559478-T-C

http://identifiers.org/hco/11/GRCh38#134489611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26559409-A-C

134489635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559385-T-C

134498204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558467-T-C

134498281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558370-G-A

http://identifiers.org/hco/11/GRCh38#134500972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26554529-C-A

134501372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26554162-G-A

http://identifiers.org/hco/11/GRCh38#134501520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26554041-C-A

134501803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553783-C-T

134501966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553609-G-A

134501973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553602-C-T

134502068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553512-G-T

134502215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553381-G-A

134502344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553257-G-A

134502363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553238-C-T

http://identifiers.org/hco/11/GRCh38#134502568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26553004-C-A

134502568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553004-C-T

134502569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26553003-G-A

134502728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26552872-A-G

http://identifiers.org/hco/11/GRCh38#134502907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26552696-A-C

134503154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552459-G-A

134503154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552459-G-T

134503204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552426-G-A

134503204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552426-G-T

134503345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552283-G-A

134503345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552283-G-T

134503382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552248-A-G

http://identifiers.org/hco/11/GRCh38#134503394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26552236-C-A

134503427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552203-G-A

134503427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552203-G-T

http://identifiers.org/hco/11/GRCh38#134503495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26552142-C-A

134503495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26552142-C-T

134503741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551931-T-C

134503824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551883-T-G

134503952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551724-G-T

134503956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551720-G-C

134503956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551720-G-T

http://identifiers.org/hco/11/GRCh38#134504002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26551676-C-A

http://identifiers.org/hco/11/GRCh38#134504004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26551674-C-A

134504004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551674-C-T

134504114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551578-T-C

134504129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551562-G-A

134504236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551467-G-A

134504301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551403-A-G

134504301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26551403-A-T

http://identifiers.org/hco/11/GRCh38#134505302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26550522-C-A

134505302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26550522-C-T

http://identifiers.org/hco/11/GRCh38#134505319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26550505-C-A

134505322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26550502-C-T

134505330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26550494-T-C

134505597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26550296-C-G

134505597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27449
most severe consequence: non coding transcript exon variant
orthologous variants: 26550296-C-T