http://identifiers.org/hco/7/GRCh38#77122478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21629823-C-A

77122478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21629823-C-T

77122528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21629764-G-T

77122805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21629487-A-G

77122951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21629144-C-T

77123041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21629039-A-G

77123221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21628870-T-G

77123678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21628350-C-T

77123966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21627383-A-G

77124045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21627311-T-G

77124176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21627180-A-G

77124215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21627140-A-G

77124299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21627058-T-C

77124437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21626957-C-T

77124491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21626893-T-G

77124574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21626830-T-A

77125137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21626401-T-G

77125216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21626283-C-T

77125443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, undefined
orthologous variants: 21626051-A-G

77125454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21626040-G-A

77125621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21625879-C-G

77125754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21625719-C-T

77125895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21625581-T-C

77126124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21625427-G-A

77126215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21625346-T-C

77127569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625150-T-C

77127585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625134-A-G

77127642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625086-T-C

http://identifiers.org/hco/7/GRCh38#77127981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21624420-C-A

http://identifiers.org/hco/7/GRCh38#77128472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21623960-A-C

77128780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623674-G-C

77128863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623597-C-T

http://identifiers.org/hco/7/GRCh38#77128867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21623593-A-C

77128867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623593-A-G

77128931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623535-G-A

77151869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620302-A-T

77152300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619761-C-T

77152601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619505-A-G

http://identifiers.org/hco/7/GRCh38#77153007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21619178-C-A

77155576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618692-T-A

77155617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618652-A-T

http://identifiers.org/hco/7/GRCh38#77155765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21618468-C-A

77156126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618196-T-A

77156126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618196-T-C

77156160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618166-A-G

77156353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618010-G-C

77156353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618010-G-T

77156746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617645-G-C

77156756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617641-T-C

77156759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617638-T-C

77156775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617622-G-T

77156844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617563-G-A

77156900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617512-A-G

77157135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617279-G-A

http://identifiers.org/hco/7/GRCh38#77157183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21617231-C-A

77157461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616978-T-G

77157497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616612-C-T

77157681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616309-T-C

77157917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616098-A-G

77157917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616098-A-T

77166284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21605677-A-G

77166446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21605564-C-T

77166545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21605464-G-A

77166823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21605201-G-T

77166828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21605197-C-T

77167591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21604906-T-A

77167591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21604906-T-C

77167625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21604878-T-A

77167625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21604878-T-G

http://identifiers.org/hco/7/GRCh38#77167635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21604868-C-A

77167635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21604868-C-T

77167735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant
orthologous variants: 21604702-C-T

77167795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant
orthologous variants: 21604642-G-A

77172431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21602097-G-T

77172666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21601873-T-C

77172867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21601690-G-A

77172929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21601631-A-G

77172936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21601624-G-A

77174129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21600938-T-C

77174192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21600882-G-A

77174249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21600825-T-A

77175469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21600291-G-A

77175527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21600234-T-A

77175851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21597086-G-T

77175879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21597057-G-T

77175881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21597055-T-C

77175946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596989-A-G

77175957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596978-C-T

77176111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596845-G-A

77176151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596812-A-G

77176645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596398-C-G

77176711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596335-A-G

77176763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21596300-A-T

77177901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21595398-G-T

77178694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21594517-A-T

http://identifiers.org/hco/7/GRCh38#77178792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21594293-A-C

77179302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21593833-C-T

77181033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21590657-T-C

77181381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21590318-T-A

77181430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21590245-A-T

77181564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21590133-T-C

http://identifiers.org/hco/7/GRCh38#77182179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21589552-A-C

77182873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21589176-A-G

77182916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21589132-G-A

77183546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21588524-C-T

http://identifiers.org/hco/7/GRCh38#77183606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21588478-C-A

77183606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21588478-C-T

77183669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21588397-A-G

77183756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21588313-T-G

77184337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21587820-C-T

77184376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21587782-G-A

77184728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21587150-G-C

77185098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21586790-G-A

77185098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21586790-G-T

77188817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21585095-A-G

77189096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21584823-A-G

77189188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21584742-C-T

77189351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21584578-G-A

77189622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21584342-A-G

77189742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21584214-C-T

77189817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21584140-G-T

77193250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21583525-T-C

77193250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21583525-T-G

77193252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21583523-T-C

77193351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21583423-C-T

77193359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21583415-A-G

77193359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21583415-A-T

77193473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21583308-T-A

77193525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21583254-C-T

http://identifiers.org/hco/7/GRCh38#77193546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21583238-C-A

77194302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21582581-A-G

77194424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21582464-T-C

77194495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21582397-G-T

http://identifiers.org/hco/7/GRCh38#77194578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21582298-C-A

77194579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21582297-T-C

77195064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581795-A-G

77195066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581793-G-T

http://identifiers.org/hco/7/GRCh38#77195084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21581775-A-C

77195116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581742-G-T

77195135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581729-T-C

http://identifiers.org/hco/7/GRCh38#77195160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21581709-C-A

77195160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581709-C-T

77195190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581686-T-C

77195190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581686-T-G

http://identifiers.org/hco/7/GRCh38#77195214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21581675-C-A

77195214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581675-C-T

77195238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581651-A-G

77196101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581118-G-A

77196101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581118-G-T

77196148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581077-T-G

http://identifiers.org/hco/7/GRCh38#77196175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21581065-C-A

77196176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21581064-A-G

http://identifiers.org/hco/7/GRCh38#77196237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21580999-C-A

77196237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21580999-C-T

77196254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21580982-T-C

77196586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21580649-G-A

77196739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21580496-T-C

77196841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21580394-A-G

77196921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21580314-G-T

77197014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21580213-G-T

77197036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21580191-C-T

77197072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21580158-G-T

77197096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21580127-G-A

77197123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21580092-G-A

77197123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21580092-G-T

77197368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579880-G-A

77197368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579880-G-T

77197509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579737-C-T

77197629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579661-G-A

77197673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579626-C-T

77197969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579327-A-G

77198044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579263-A-G

77198054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579253-A-G

77198241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579117-T-A

77198241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21579117-T-C

77198448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578995-G-T

77198494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578959-A-G

http://identifiers.org/hco/7/GRCh38#77198693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21578737-C-A

77198714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578715-G-A

77198714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578715-G-T

77198716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578713-T-G

77198718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578711-A-G

77198964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578513-G-T

77199001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578476-A-T

77199003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578474-T-G

77199121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578362-G-T

77199144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21578339-T-C

77199417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21578068-C-G

77199417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21578068-C-T

77199437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21578051-T-C

77199727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21577776-C-G

77199756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21577750-A-G

http://identifiers.org/hco/7/GRCh38#77199809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21577699-C-A

77199809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21577699-C-T

77199853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577668-G-A

77199853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577668-G-T

77199865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577656-G-A

77199865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577656-G-C

77199865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577656-G-T

77199920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577602-G-T

77199960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577564-T-C

77200036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577486-C-T

http://identifiers.org/hco/7/GRCh38#77200123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21577402-A-C

77200126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577399-A-G

77200333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21577209-G-A

77200966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576874-T-C

77201042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576681-C-T

77201689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576434-C-T

77201692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576431-C-T

77201698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576425-T-C

77201742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576392-A-G

77201813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576353-T-G

77201880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576291-T-A

77201946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576237-A-G

77202006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576202-T-G

77202178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21576049-C-T

77202274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21575932-G-C

77207011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21574352-A-G

77207075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21574301-A-G

77207075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21574301-A-T

http://identifiers.org/hco/7/GRCh38#77207413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21574010-C-A

77207413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21574010-C-G

77207425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21573998-G-A

77207557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21573864-A-G

77208021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21573500-G-C

77208170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21572907-T-C

77208196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21572881-C-G

77208237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21572840-G-A

77215578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21565168-T-G

77215582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21565164-T-C

http://identifiers.org/hco/7/GRCh38#77215596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21565149-C-A

77215645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21565109-C-T

77215818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21564945-G-A

77215818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21564945-G-C

77215841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21564922-A-G

http://identifiers.org/hco/7/GRCh38#77216081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21564686-C-A

77216133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21564646-T-C

77216179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21564602-T-C

77216412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21564159-T-C

77216698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21563814-T-G

77216857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21563667-G-A

77216971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21563575-T-G

77217039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21563507-A-G

77217212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21563339-G-T

77219006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21562281-G-A

77219334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21561973-A-G

77219334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21561973-A-T

77219347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21561956-T-C

77219349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron variant
orthologous variants: 21561954-G-T

77221604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21560684-C-T

77221688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21560620-A-T

77221704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21560606-T-C

77221743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21560567-T-C

77222035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21560291-G-C

http://identifiers.org/hco/7/GRCh38#77222240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21560079-C-A

77222240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21560079-C-T

77222457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559829-C-T

77222818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559487-G-A

77222818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559487-G-T

77222902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559396-A-G

77222951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559349-T-C

77223036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559273-C-T

77223097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21559216-A-G

77223261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558934-C-T

77223276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558918-A-G

77223527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558663-C-G

http://identifiers.org/hco/7/GRCh38#77223684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21558509-A-C

77223824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558366-G-A

77224074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558038-A-G

77224076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21558036-A-G

77224359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557787-T-C

77224445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557706-G-A

77224466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557685-T-A

77224477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557674-T-C

77224503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557647-C-T

77224548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557603-T-C

77224659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557505-A-G

77224725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21557441-T-C

77226295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21553496-T-C

http://identifiers.org/hco/7/GRCh38#77226296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21553495-C-A

77226296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21553495-C-T

77226404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21553414-C-T

77226405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21553413-G-A

77226569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21553264-T-A

77226858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21552971-T-C

77226888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21552941-A-G

http://identifiers.org/hco/7/GRCh38#77227295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21552263-A-C

77236568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21538541-A-G

http://identifiers.org/hco/7/GRCh38#77236921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21538213-C-A

77236921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21538213-C-T

77237174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537872-A-G

77237307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537761-T-C

77237421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537664-G-A

77237421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537664-G-T

77237438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537647-A-T

77237480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537626-G-A

77237481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537625-G-A

77238817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537422-A-G

77239141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537111-A-G

77239179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21537071-A-G

77239376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536899-T-C

http://identifiers.org/hco/7/GRCh38#77239432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21536843-C-A

77239578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536732-G-A

77239746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21536561-T-C

77240358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535928-C-T

77241651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535785-A-G

77241651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21535785-A-T

77241713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21535723-C-T

http://identifiers.org/hco/7/GRCh38#77241854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21535582-A-C

77242161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21535185-A-G

http://identifiers.org/hco/7/GRCh38#77242229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21535133-C-A

77242242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21535115-T-A

77242242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21535115-T-C

77242242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21535115-T-G

77242320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21535079-G-A

77242431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 21534994-G-A

77242431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 21534994-G-C

77242431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 21534994-G-T

77242453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534972-T-G

77242517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534914-G-T

77242524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534905-T-A

http://identifiers.org/hco/7/GRCh38#77242554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21534881-C-A

77242626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534851-G-A

77242951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534542-A-G

77243165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534327-A-T

77243275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534206-G-A

77243299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21534182-G-A

77245159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21533268-A-G

77245346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21533144-G-C

77245346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21533144-G-T

77245438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21533059-G-T

77245507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532991-A-G

77245509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532989-G-A

77245668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532852-T-G

77246625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532433-G-C

77246650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532417-T-C

77246720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532345-A-G

77246834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21532207-A-G

77247413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21531672-A-T

77247460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21531643-G-A

77252791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21529353-C-G

77252791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21529353-C-T

77253036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21529151-G-A

77253412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528970-G-T

77253480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528905-G-A

77253480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528905-G-T

http://identifiers.org/hco/7/GRCh38#77253631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21528763-A-C

77253698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528694-G-T

77253708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528685-T-A

77253708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528685-T-C

77253743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528660-G-A

77253891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528587-G-A

77253929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528556-G-A

77254358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528019-T-A

77254358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528019-T-C

77254358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21528019-T-G

77254380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527964-T-A

77254380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527964-T-C

77254410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527936-G-C

77254410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527936-G-T

77254411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527935-G-A

77254411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527935-G-C

77254411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527935-G-T

77254427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527887-A-G

77254445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527859-G-C

77254445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527859-G-T

77254529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21527774-T-C

77254583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527729-G-C

77254583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527729-G-T

77254584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527728-A-G

http://identifiers.org/hco/7/GRCh38#77254650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21527680-A-C

77254650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527680-A-G

http://identifiers.org/hco/7/GRCh38#77254667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21527663-A-C

77254667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527663-A-G

77254676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527655-A-G

77254676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527655-A-T

77254704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527637-A-T

77254750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527593-T-C

77254757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527586-T-C

77254766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527578-G-A

77254779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527565-G-C

77254896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527447-C-G

77254924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21527429-A-G

http://identifiers.org/hco/7/GRCh38#77255673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21526882-C-A

77255818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526780-G-A

77256013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526613-T-C

77256130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526513-A-G

http://identifiers.org/hco/7/GRCh38#77256215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21526454-C-A

77256233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526436-T-A

77256233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526436-T-C

77256233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526436-T-G

77256285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526383-A-T

77256301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526367-A-G

77256348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21526321-A-G

77256348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21526321-A-T

77256480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 21526189-G-T

77256511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 21526158-T-A

http://identifiers.org/hco/7/GRCh38#77256536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21526129-A-C

77256567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526101-T-C

77256602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526069-G-A

77256655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21526031-T-C

77256774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525912-A-G

http://identifiers.org/hco/7/GRCh38#77256797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21525889-C-A

http://identifiers.org/hco/7/GRCh38#77257179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21525854-C-A

77257179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525854-C-G

77257179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525854-C-T

http://identifiers.org/hco/7/GRCh38#77257232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21525800-C-A

77257532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525535-A-G

77257553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525514-G-A

77257553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525514-G-C

77257686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525390-C-T

77257769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525308-G-A

77257770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525307-G-T

77257784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525293-A-G

77257880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21525215-G-T

77257900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21525196-C-T

77257909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21525187-G-T

77257955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21525141-T-C

77257959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21525110-G-T

77258049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21525036-A-G

http://identifiers.org/hco/7/GRCh38#77258194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21524880-C-A

77258194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524880-C-G

77258194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524880-C-T

77258205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524869-A-G

http://identifiers.org/hco/7/GRCh38#77258208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21524866-C-A

77258208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524866-C-T

77258870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524704-G-C

77258904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524669-T-A

77258998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524595-G-A

77259095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524498-T-C

77259100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524493-G-C

77259100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524493-G-T

77259119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524465-G-A

77259119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524465-G-C

77259119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524465-G-T

77259177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524430-A-T

77259233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524374-T-A

77259233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21524374-T-C

77259328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524314-T-C

77259408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524247-A-G

77259411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524244-C-T

77259568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524106-T-A

77259568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21524106-T-C

77259986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21523232-G-A

77260100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21523118-G-A

77260169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21523049-G-A

http://identifiers.org/hco/7/GRCh38#77260268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21522955-C-A

77260268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522955-C-T

77260294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522930-T-A

77260294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522930-T-C

77260346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522873-A-T

77260351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522868-A-T

77260375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522838-T-A

77260398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522819-T-C

77260513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522714-T-C

77260685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522505-G-A

77260693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522497-C-G

77260815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522367-G-A

77260815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522367-G-C

77260850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522325-G-A

77260850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522325-G-T

77260917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522236-C-T

77261096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522062-T-C

77261096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21522062-T-G

77262200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21521889-G-A

77262300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21521789-T-A

77262385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521709-T-C

http://identifiers.org/hco/7/GRCh38#77262451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21521654-C-A

77262831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521265-C-T

77262873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521221-C-G

77262954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521144-G-A

77263057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21521034-T-C

77263195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520908-C-T

http://identifiers.org/hco/7/GRCh38#77263199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21520904-C-A

77264947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21520210-T-A

77269921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21518797-G-A

http://identifiers.org/hco/7/GRCh38#77269977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21518748-C-A

77270046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21518694-G-A

77270229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21518511-A-G

77270261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21518479-A-G

77270835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21517953-C-T

77271865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21516280-C-T

77271977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21516179-C-T

77272455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515801-T-C

77272762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515513-T-C

77273052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515150-A-G

77273120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515070-C-T

77273188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515016-T-A

77273197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515008-T-A

77273197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21515008-T-C

77273360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514863-T-C

77273494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514731-C-T

77273677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514701-T-A

77273689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21514689-T-C

77273873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21514515-T-C

http://identifiers.org/hco/7/GRCh38#77274130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21514275-A-C

77274418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21513835-A-T

77274469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21513792-T-G

77275405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21513363-G-A

77275978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512793-G-A

77276104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512700-A-G

77276589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512372-A-G

77276590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512371-T-C

77276590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512371-T-G

77277214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512094-C-T

77277238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21512069-C-G

77277314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21511991-A-G

77277394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21511912-A-G

77277429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21511879-C-G

http://identifiers.org/hco/7/GRCh38#77277506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21511803-A-C

77277523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21511786-G-A

77277523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21511786-G-C

http://identifiers.org/hco/7/GRCh38#77277566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21511740-A-C

77277605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21511688-A-G

77277948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21511304-T-C

77278112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21511129-A-T

http://identifiers.org/hco/7/GRCh38#77278143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21511100-C-A

77278203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21511044-C-T

http://identifiers.org/hco/7/GRCh38#77278223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21511024-C-A

77278258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21511004-T-C

77278589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21510688-G-T

77278893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21510455-A-T

77279706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508890-C-T

77280123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508500-G-A

77280123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508500-G-T

77280166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508462-C-T

http://identifiers.org/hco/7/GRCh38#77280407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21508306-C-A

77280407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508306-C-T

77280646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21508067-A-T

http://identifiers.org/hco/7/GRCh38#77280681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21508028-C-A

77280681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21508028-C-T

http://identifiers.org/hco/7/GRCh38#77280764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21507998-C-A

77280764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507998-C-T

77280787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507979-C-T

77281400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507536-G-A

77281522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507410-T-C

77281552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507394-T-C

77281552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507394-T-G

77281818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507125-A-G

77281828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507115-G-A

77281835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507108-A-G

77281866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507070-A-G

77281917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507014-G-A

77281961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21507003-G-A

77282162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21506825-G-T

http://identifiers.org/hco/7/GRCh38#77282235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506761-C-A

http://identifiers.org/hco/7/GRCh38#77282236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506760-A-C

77282236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21506760-A-G

77282241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21506755-A-G

77282299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506700-T-C

77282299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506700-T-G

77282310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506688-A-G

http://identifiers.org/hco/7/GRCh38#77282369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506633-C-A

77282369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506633-C-T

http://identifiers.org/hco/7/GRCh38#77282439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506565-C-A

77282439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506565-C-T

77282465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506544-T-C

http://identifiers.org/hco/7/GRCh38#77282495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506514-A-C

77282495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506514-A-G

http://identifiers.org/hco/7/GRCh38#77282541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506468-C-A

77282541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21506468-C-T

77282549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21506460-G-A

77282549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21506460-G-T

http://identifiers.org/hco/7/GRCh38#77282550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506459-A-C

77282550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21506459-A-G

http://identifiers.org/hco/7/GRCh38#77282799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506210-C-A

http://identifiers.org/hco/7/GRCh38#77282818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21506191-C-A

77282854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21506148-G-T

77284662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504423-A-G

77284685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504400-T-C

77284741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504344-C-T

77284840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504244-T-A

77284879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504183-A-G

77284879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504183-A-T

77284973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504107-T-C

77285053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504018-G-A

77285053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21504018-G-T

77285172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21503894-C-T

http://identifiers.org/hco/7/GRCh38#77285174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21503892-C-A

77285576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21503208-T-C

77285685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21503120-C-T

http://identifiers.org/hco/7/GRCh38#77285880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502955-A-C

77285940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502910-T-C

77286533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502767-T-C

http://identifiers.org/hco/7/GRCh38#77287044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502484-A-C

http://identifiers.org/hco/7/GRCh38#77287052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502478-C-A

77287052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502478-C-T

77287064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502466-A-G

77287064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502466-A-T

77287080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502450-T-C

77287080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502450-T-G

http://identifiers.org/hco/7/GRCh38#77287095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502437-C-A

77287095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502437-C-T

77287140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502393-G-A

77287140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502393-G-T

http://identifiers.org/hco/7/GRCh38#77287149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502384-C-A

77287149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21502384-C-T

77287236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502295-G-A

77287236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502295-G-T

http://identifiers.org/hco/7/GRCh38#77287244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502287-A-C

77287244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502287-A-T

77287255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502277-G-C

77287255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502277-G-T

77287262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21502270-T-A

http://identifiers.org/hco/7/GRCh38#77287369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21502140-C-A

http://identifiers.org/hco/7/GRCh38#77287591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21501910-C-A

77287785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21501495-C-T

77288802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21500885-C-G

77289307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21500448-C-T

77292802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499838-C-T

77292835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499809-A-T

77292902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499747-G-T

77292931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499718-C-T

77293194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21499455-G-T

77293334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499052-G-A

77293334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499052-G-T

77293381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21499008-C-T

77293433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21498966-T-A

77293441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21498958-T-C

77294596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21498553-G-A

77294596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21498553-G-C

77294596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21498553-G-T

http://identifiers.org/hco/7/GRCh38#77294608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21498542-A-C

77294674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21498480-A-G

77294679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21498475-A-G

77294774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21498380-C-T

77294810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21498344-C-G

77294810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21498344-C-T

http://identifiers.org/hco/7/GRCh38#77294909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21498242-C-A

77294909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21498242-C-T

77295089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21498072-A-G

77295135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21498025-T-C

77295135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21498025-T-G

77309667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21497539-C-T

77309914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21497254-C-T

77309917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21497251-T-C

77310007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21497087-G-A

77310184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496915-T-C

77310196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496903-C-T

77310236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496864-C-T

77310488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496449-T-C

77310580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496357-G-A

77310620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496319-A-G

77310660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496279-G-T

http://identifiers.org/hco/7/GRCh38#77310682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21496256-C-A

77310682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496256-C-T

77310686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496252-G-C

http://identifiers.org/hco/7/GRCh38#77310691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21496247-A-C

77310691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496247-A-G

77310695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21496243-T-C

77310925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21496006-T-G

77311119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495830-T-C

http://identifiers.org/hco/7/GRCh38#77311204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495756-C-A

77311230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495730-C-T

77311326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495647-T-G

http://identifiers.org/hco/7/GRCh38#77311340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495643-C-A

77311340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495643-C-G

77311340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495643-C-T

77311374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495609-A-G

77311413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 21495570-G-A

http://identifiers.org/hco/7/GRCh38#77311442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495541-A-C

http://identifiers.org/hco/7/GRCh38#77311445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495538-C-A

77311445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21495538-C-T

77311466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495517-A-G

77311486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495452-T-C

77311503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495436-A-G

77311506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495433-T-C

77311639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495325-T-C

77311649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495315-T-A

77311684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495283-T-C

http://identifiers.org/hco/7/GRCh38#77311722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495248-C-A

77311786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495186-G-T

77311789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495183-T-C

http://identifiers.org/hco/7/GRCh38#77311858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495123-A-C

77311858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495123-A-G

77311858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495123-A-T

77311894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495087-A-G

77311894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495087-A-T

77312052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21494932-A-G

77312114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21494873-T-C

77312234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494755-T-A

77312319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494666-G-A

77312319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494666-G-T

77312343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494642-G-T

77312526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494466-G-A

77313033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494050-C-T

77313073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494010-C-T

77313184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493905-C-T

77313294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493799-G-A

77313318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493777-G-T

77313400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493723-A-T

77313401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493722-A-G

77313436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493690-A-G

77313438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493688-G-T

77313533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21493600-C-T

http://identifiers.org/hco/7/GRCh38#77313670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21493464-C-A

77313670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493464-C-G

77313921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493218-T-C

77313923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493216-G-T

77314135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492999-T-C

77314178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492970-A-G

77314267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492883-T-A

77314267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492883-T-C

77314267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492883-T-G

http://identifiers.org/hco/7/GRCh38#77314272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21492878-C-A

77314272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492878-C-T

77314301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492860-C-T

77314432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492730-A-G

77314520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492640-G-T

77314542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492618-C-T

77314559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492602-G-T

77314580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492577-A-G

77314595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492565-G-T

77314688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492530-T-A

77314695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492523-A-G

77314823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492488-G-C

77314876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492435-G-A

77314876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492435-G-T

http://identifiers.org/hco/7/GRCh38#77314892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21492416-C-A

77314892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492416-C-T

http://identifiers.org/hco/7/GRCh38#77315001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21492318-A-C

77315002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492317-G-A

77315064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492244-A-G

77315177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492137-G-A

77315183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492131-G-A

77315201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492117-A-G

77315208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492110-A-G

77315241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492087-A-G

77315361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491979-C-G

77315366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491974-G-T

77315455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491893-A-G

http://identifiers.org/hco/7/GRCh38#77315461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21491887-C-A

77315511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491847-G-T

77315611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491755-T-C

77315725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491629-G-C

77315928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491445-G-T

77316124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491245-T-G

77316183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491217-G-T

http://identifiers.org/hco/7/GRCh38#77316186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21491214-C-A

77316186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491214-C-T

77316240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21488999-G-T

77316608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21488650-C-G

77316711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21488563-C-T

77316725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21488543-A-G

77319131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487870-A-G

77319152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487847-A-G

77319287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487723-T-C

77319421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487601-T-C

77319601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487423-A-T

77319785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487228-G-C

77319809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487204-T-G

77319913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487091-A-G

77319940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487065-G-A

77319940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487065-G-T

77320181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486895-C-T

77320219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486859-T-C

77320584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486712-G-C

77320584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486712-G-T

77320652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486659-G-T

77320724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 21486599-C-T

77320935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486406-A-G

77320936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486405-T-G

http://identifiers.org/hco/7/GRCh38#77320958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21486383-A-C

77321263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486146-A-G

77321263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486146-A-T

77321264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486145-G-A

77321264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486145-G-T

77321440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485955-T-G

http://identifiers.org/hco/7/GRCh38#77321473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21485923-C-A

77321496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485899-G-T

http://identifiers.org/hco/7/GRCh38#77321513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21485882-C-A

77321513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485882-C-T

77321947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485465-T-C

77322031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485368-G-A

77322108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485290-A-G

77322136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485259-A-G

77322483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484988-G-A

77322527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484947-G-A

77322984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483459-G-A

77323570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483210-T-A

77323570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483210-T-C

77323612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483173-A-G

77323612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483173-A-T

77323614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483171-G-A

77323614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483171-G-T

77323616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483169-G-A

77323616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483169-G-T

http://identifiers.org/hco/7/GRCh38#77323617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21483168-C-A

77323617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483168-C-T

77323631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483152-A-G

77323760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483023-A-G

77323802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482981-T-C

77323811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482967-A-G

http://identifiers.org/hco/7/GRCh38#77323878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21482895-C-A

77323878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482895-C-T

77323880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482893-T-C

77324107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479739-C-T

77324141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479705-A-T

77324168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479665-G-C

77324411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479363-T-G

http://identifiers.org/hco/7/GRCh38#77324496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21479262-A-C

77324496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479262-A-T

77324576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479211-G-C

http://identifiers.org/hco/7/GRCh38#77326172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21478078-C-A

77326172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21478078-C-T

77326595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477895-A-G

77326595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477895-A-T

http://identifiers.org/hco/7/GRCh38#77326614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21477877-A-C

77326724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477770-G-A

77326724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477770-G-T

77326830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477686-G-A

77326830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477686-G-T

77327070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477470-G-A

http://identifiers.org/hco/7/GRCh38#77327121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21477421-C-A

77327121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477421-C-G

77327121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477421-C-T

77327170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477381-C-G

77327170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477381-C-T

77327180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477371-G-A

77327180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477371-G-T

77327205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477350-A-G

http://identifiers.org/hco/7/GRCh38#77327250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21477315-C-A

77327250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477315-C-T

77327411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477229-T-C

77327809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21476874-A-G

77328141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21476674-T-C

77328142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21476673-T-C

77328172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476643-G-A

77328172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476643-G-T

http://identifiers.org/hco/7/GRCh38#77328306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21476527-C-A

77328306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476527-C-T

http://identifiers.org/hco/7/GRCh38#77328373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21476470-C-A

77328373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476470-C-T

77328382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476461-T-C

77328444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476399-G-A

77328444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476399-G-C

77328444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476399-G-T

http://identifiers.org/hco/7/GRCh38#77328575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#21476271-C-A

77328628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 21476222-A-T

http://identifiers.org/hco/7/GRCh38#77329048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475809-C-A

77329264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21475646-A-G

77329360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475583-A-G

77329360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475583-A-T

http://identifiers.org/hco/7/GRCh38#77329405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475538-C-A

77329405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475538-C-G

77329405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475538-C-T

http://identifiers.org/hco/7/GRCh38#77329481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475455-C-A

77329481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475455-C-T

77329503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29296
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475437-T-G