http://identifiers.org/hco/6/GRCh38#34792096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#28075568-A-C

34792096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075568-A-G

34792096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075568-A-T

34792114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075586-G-A

34792114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075586-G-T

34792134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075606-G-A

34792134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075606-G-T

34792135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28075607-C-T

34792330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28075795-G-A

34792330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28075795-G-T

http://identifiers.org/hco/6/GRCh38#34792331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28075796-C-A

34792331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28075796-C-T

http://identifiers.org/hco/6/GRCh38#34792370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28075829-C-A

34792370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28075829-C-T

http://identifiers.org/hco/6/GRCh38#34792421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28075853-C-A

34792421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28075853-C-G

34792421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28075853-C-T

34792789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28076076-G-A

34792789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28076076-G-T

34792982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28076255-A-G

34793073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28076350-T-A

34793198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28076457-G-A

34795752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28078051-C-T

34795801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28078103-A-G

34795805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28078107-C-T

34796359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28078483-G-A

34796387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28078510-G-A

http://identifiers.org/hco/6/GRCh38#34797001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28079264-C-A

34797001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079264-C-G

34797080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079345-G-A

34797102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079362-G-A

34797296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079493-A-G

34797325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079513-T-A

34797342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079534-T-G

34797348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079540-A-G

34797348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079540-A-T

34797404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079623-T-A

34797404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079623-T-C

34797409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079628-G-C

34797665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079837-T-G

http://identifiers.org/hco/6/GRCh38#34797725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28079908-A-C

34797725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28079908-A-G

34797966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28080135-T-C

34798113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28080282-C-G

34801401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28086531-G-T

34801423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28086555-A-T

http://identifiers.org/hco/6/GRCh38#34801452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28086582-C-A

34813853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28091336-G-C

34813902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28091352-G-C

34813913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28091363-A-G

http://identifiers.org/hco/6/GRCh38#34813955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28091384-C-A

http://identifiers.org/hco/6/GRCh38#34813958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28091387-A-C

http://identifiers.org/hco/6/GRCh38#34813959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28091388-A-C

34813959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28091388-A-T

34814090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28091481-C-T

34814635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28092103-G-A

34814694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28092165-G-C

34817362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28094008-C-G

34817362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28094008-C-T

34821589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28095571-G-T

34821779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28095763-C-T

34821814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 28095798-G-A

34821835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28095818-T-C

34821878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28095859-C-G

34821946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28095927-T-C

http://identifiers.org/hco/6/GRCh38#34823200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28096247-C-A

34823200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28096247-C-T

34823295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28096334-G-A

34823356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28096395-T-G

34834197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098178-G-A

34834352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28098333-C-T

34834443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098425-G-T

http://identifiers.org/hco/6/GRCh38#34834445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28098427-A-C

http://identifiers.org/hco/6/GRCh38#34834635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28098570-C-A

34834635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098570-C-T

34834639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098574-G-A

34834639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098574-G-T

34834816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28098720-G-C

34834928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098807-A-G

34835060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098880-G-A

34835108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28098929-G-T

34835226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron_variant, undefined
orthologous variants: 28099042-G-A

34835226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron_variant, undefined
orthologous variants: 28099042-G-C

34835226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron_variant, undefined
orthologous variants: 28099042-G-T

34835231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron_variant, undefined
orthologous variants: 28099049-A-G

34835259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099077-G-C

34835350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28099165-C-G

http://identifiers.org/hco/6/GRCh38#34835434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28099249-A-C

34835434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28099249-A-G

34835456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28099271-C-T

34835477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099292-A-G

34835518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099331-C-T

34835532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099345-T-C

http://identifiers.org/hco/6/GRCh38#34835586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28099606-C-A

34835628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099649-C-T

34835698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099716-G-A

http://identifiers.org/hco/6/GRCh38#34835706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28099724-C-A

34835761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099779-G-A

34835921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099899-A-G

http://identifiers.org/hco/6/GRCh38#34836024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28099992-C-A

34836024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28099992-C-T

http://identifiers.org/hco/6/GRCh38#34836051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28100027-C-A

http://identifiers.org/hco/6/GRCh38#34836070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28100043-C-A

34836119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100091-G-A

34836119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100091-G-T

34836122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100094-C-T

34836361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100600-G-T

34836372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100610-G-C

34836380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100618-G-T

34836416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100654-G-A

34836467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100712-T-A

34836467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100712-T-C

34836467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28100712-T-G

34855535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28102914-A-G

34855595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28102973-C-T

34855602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28102980-A-G

34855675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28103053-G-A

http://identifiers.org/hco/6/GRCh38#34855799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28103150-C-A

http://identifiers.org/hco/6/GRCh38#34855817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28103168-C-A

34855817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103168-C-T

34856027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103288-A-G

34856208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103378-G-A

34856411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: splice donor variant
orthologous variants: 28103580-T-C

34856638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103756-A-G

34856644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103762-T-C

34856652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103767-T-C

http://identifiers.org/hco/6/GRCh38#34856654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28103771-C-A

34856654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28103771-C-T

http://identifiers.org/hco/6/GRCh38#34856658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28103775-C-A

http://identifiers.org/hco/6/GRCh38#34856944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28104041-A-C

34857019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104093-G-A

34857019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104093-G-T

34857026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104100-T-C

http://identifiers.org/hco/6/GRCh38#34857177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28104280-A-C

34857177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104280-A-G

34857177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104280-A-T

http://identifiers.org/hco/6/GRCh38#34857187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28104290-A-C

34857187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104290-A-G

http://identifiers.org/hco/6/GRCh38#34857188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28104291-C-A

34857288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104340-A-T

34857293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104345-G-A

34857293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104345-G-C

34857424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28104476-T-C

http://identifiers.org/hco/6/GRCh38#34857631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28104789-C-A

34857631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104789-C-G

34857631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104789-C-T

34857665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104821-A-G

34857691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28104847-C-T

34857779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28104930-T-C

34857779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28104930-T-G

http://identifiers.org/hco/6/GRCh38#34857890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28105041-C-A

34857958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28105108-C-T

34858092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28105205-A-G

34858416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28105508-C-G

34858416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28105508-C-T

34858611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28105703-C-G

34858612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28105704-A-G

http://identifiers.org/hco/6/GRCh38#34858732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28105824-A-C

34858823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28105918-C-G

34858823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28105918-C-T

34859034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28106129-C-G

34859034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28106129-C-T

34859038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28106133-C-G

34859038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28106133-C-T

34859131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28106226-C-T

34859330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28106425-T-A

34859330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28106425-T-C

34859416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28106511-T-C

34859416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28106511-T-G

34859597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28106697-T-C

34859597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28106697-T-G

http://identifiers.org/hco/6/GRCh38#34859647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28106746-C-A

34859647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28106746-C-G

34859647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28106746-C-T

34859713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28106923-T-G

34859850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28107089-C-T

34859997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28107182-T-C

34859997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28107182-T-G

34860072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28107236-G-T

34860143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28107303-G-A

34863741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28108807-A-G

34863934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28108930-T-G

34864002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 28108974-G-A

34864002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 28108974-G-T

34864023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28108995-T-G

34864039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28109011-C-T

http://identifiers.org/hco/6/GRCh38#34864119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28109091-A-C

34864119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28109091-A-G

http://identifiers.org/hco/6/GRCh38#34864229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28109191-A-C

34864285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28109245-G-A

34864285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28109245-G-T

http://identifiers.org/hco/6/GRCh38#34864308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28109268-C-A

34864308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28109268-C-T

http://identifiers.org/hco/6/GRCh38#34867086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28112007-A-C

34867086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112007-A-T

34867199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112080-A-G

34867265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28112155-T-C

http://identifiers.org/hco/6/GRCh38#34867368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28112255-A-C

34867376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28112263-C-T

34867392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112279-A-G

34867416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112297-C-G

34867426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112307-A-G

34867609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28112496-G-A

34867653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112536-C-G

34867704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112586-G-A

34867704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112586-G-C

http://identifiers.org/hco/6/GRCh38#34867708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28112590-C-A

34867708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112590-C-G

34867708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112590-C-T

http://identifiers.org/hco/6/GRCh38#34867737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28112623-C-A

34867737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112623-C-T

34867872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28112727-A-G

34870393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113100-T-A

34870559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113244-C-G

34870712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113382-A-G

34870716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113386-A-T

34870745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113413-G-T

http://identifiers.org/hco/6/GRCh38#34870759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28113426-C-A

http://identifiers.org/hco/6/GRCh38#34870765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28113435-C-A

34870765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113435-C-T

34870770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113440-G-T

34870792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113465-T-A

34870792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28113465-T-C

34870867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28113534-G-A

34870867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28113534-G-T

34870933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28113600-T-C

http://identifiers.org/hco/6/GRCh38#34870954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28113621-C-A

34870954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28113621-C-G

34870954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28113621-C-T

34871421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114076-T-C

34871434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114089-A-G

34871434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114089-A-T

http://identifiers.org/hco/6/GRCh38#34871598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28114258-C-A

34871598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28114258-C-G

34871598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28114258-C-T

34871646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: synonymous variant
orthologous variants: 28114306-A-G

34871790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114407-C-T

34871848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: missense variant
orthologous variants: 28114463-G-A

http://identifiers.org/hco/6/GRCh38#34871942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28114550-A-C

34871942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114550-A-G

http://identifiers.org/hco/6/GRCh38#34871992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28114587-C-A

34871992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114587-C-T

34871996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114591-G-C

34872017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114605-G-A

http://identifiers.org/hco/6/GRCh38#34872065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28114619-C-A

34872065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114619-C-T

34872152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114703-A-G

34872180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114731-G-T

http://identifiers.org/hco/6/GRCh38#34872230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28114774-C-A

34872235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: intron variant
orthologous variants: 28114779-C-T

34872580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115090-G-A

34872580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115090-G-T

http://identifiers.org/hco/6/GRCh38#34872589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28115099-C-A

34872616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115124-G-A

34872616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115124-G-C

34872616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115124-G-T

34872634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115141-T-C

34872681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115162-A-G

34872681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28115162-A-T

http://identifiers.org/hco/6/GRCh38#34872784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28115263-C-A

http://identifiers.org/hco/6/GRCh38#34872879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28115357-C-A

34875316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117192-G-A

34875335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117211-A-G

34875369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117242-T-C

34875393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117266-T-C

http://identifiers.org/hco/6/GRCh38#34875431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28117287-C-A

34875431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117287-C-T

http://identifiers.org/hco/6/GRCh38#34875451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28117306-C-A

34875451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117306-C-T

34875468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117315-C-T

http://identifiers.org/hco/6/GRCh38#34875500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28117344-C-A

34875519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117359-A-G

34875597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117421-G-T

34875673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117487-T-C

34875776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117571-A-G

34875811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117611-G-T

http://identifiers.org/hco/6/GRCh38#34875833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28117650-A-C

34875833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117650-A-G

34876249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28117968-T-C

34876306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118018-G-A

34876329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118034-A-G

34876354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118059-A-G

http://identifiers.org/hco/6/GRCh38#34876372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28118076-A-C

34876372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118076-A-G

34876377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118081-T-C

34876421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118104-G-T

http://identifiers.org/hco/6/GRCh38#34876467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28118144-C-A

34876500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118172-T-G

34876607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118197-C-T

34876681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118255-G-T

34876737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118302-T-C

34876802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118358-G-A

34876831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118389-A-G

http://identifiers.org/hco/6/GRCh38#34876837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28118395-C-A

34876837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118395-C-T

34876957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118498-G-T

34876999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118524-T-C

34877023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118547-G-T

34877056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118577-T-C

34877135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118642-G-A

http://identifiers.org/hco/6/GRCh38#34877161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28118673-C-A

34877161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118673-C-T

34877186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118711-T-G

34877267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118779-A-G

34877333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118845-A-G

http://identifiers.org/hco/6/GRCh38#34877357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28118867-C-A

34877357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: 28118867-C-T

http://identifiers.org/hco/6/GRCh38#34877402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21216
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#28118905-C-A