http://identifiers.org/hco/9/GRCh38#114333093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63283946-C-A

114333433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non coding transcript exon variant
orthologous variants: 63284207-G-A

http://identifiers.org/hco/9/GRCh38#114333449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284219-A-C

114333485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non coding transcript exon variant
orthologous variants: 63284255-A-G

114334231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284357-G-A

114334243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284369-G-C

114334270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284396-C-T

114334283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284409-G-C

114334321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284438-G-T

114334338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284449-A-G

114334349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284460-G-A

114334376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284465-G-A

114334382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284471-G-T

114334384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284473-A-G

114334388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284477-G-A

114334388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284477-G-C

114334388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284477-G-T

114334393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284482-G-T

http://identifiers.org/hco/9/GRCh38#114334395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284484-C-A

114334395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284484-C-T

114334404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284493-G-A

114334404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284493-G-T

114334411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284494-T-C

114334411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284494-T-G

114334412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284495-G-A

114334412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284495-G-T

114334413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284496-A-G

114334415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284498-G-A

114334415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284498-G-C

114334415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284498-G-T

114334419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284502-A-G

114334426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284509-G-A

114334427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284510-G-A

114334427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284510-G-C

114334427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284510-G-T

114334428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284511-G-A

114334428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284511-G-T

http://identifiers.org/hco/9/GRCh38#114334432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284515-C-A

114334432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284515-C-T

114334433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284516-A-G

http://identifiers.org/hco/9/GRCh38#114334436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284518-C-A

114334436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284518-C-T

114334439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284521-G-A

114334439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284521-G-C

114334439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284521-G-T

http://identifiers.org/hco/9/GRCh38#114334445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284527-C-A

114334445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284527-C-G

114334445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284527-C-T

114334446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284528-T-C

114334446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284528-T-G

114334458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284539-T-C

114334461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284542-A-G

114334462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284543-T-A

114334462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284543-T-C

114334462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284543-T-G

114334465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284546-G-C

114334465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284546-G-T

114334467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284548-T-A

114334467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284548-T-C

http://identifiers.org/hco/9/GRCh38#114334468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284549-C-A

114334468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284549-C-T

114334470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284551-T-A

114334470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284551-T-C

114334470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284551-T-G

114334472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284553-G-T

114334473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284554-G-T

114334474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284555-G-T

114334476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284557-G-A

114334476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284557-G-T

114334478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284559-T-C

114334522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284586-G-A

114334522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284586-G-T

http://identifiers.org/hco/9/GRCh38#114334523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284587-C-A

http://identifiers.org/hco/9/GRCh38#114334529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284591-C-A

114334529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284591-C-T

114334533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284595-G-A

114334533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284595-G-T

http://identifiers.org/hco/9/GRCh38#114334541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284603-C-A

114334541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284603-C-T

http://identifiers.org/hco/9/GRCh38#114334563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284627-C-A

114334563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284627-C-T

114334572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284629-G-A

114334572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284629-G-T

http://identifiers.org/hco/9/GRCh38#114334576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284633-C-A

114334583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284637-C-T

114334586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284640-G-A

http://identifiers.org/hco/9/GRCh38#114334590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284644-C-A

114334590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284644-C-T

114334592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284646-G-A

114334600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284654-A-G

http://identifiers.org/hco/9/GRCh38#114334605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284659-C-A

114334605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284659-C-T

http://identifiers.org/hco/9/GRCh38#114334609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284663-A-C

114334609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284663-A-G

114334618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284668-G-C

114334618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284668-G-T

114334636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284688-C-T

114334640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284692-G-A

114334640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284692-G-C

114334648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284695-T-G

114334660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63284707-T-C

http://identifiers.org/hco/9/GRCh38#114334661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63284708-C-A

http://identifiers.org/hco/9/GRCh38#114335983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285209-A-C

114335988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63285214-A-G

114335992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63285218-A-G

114336034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63285268-C-T

http://identifiers.org/hco/9/GRCh38#114336070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285303-C-A

http://identifiers.org/hco/9/GRCh38#114336095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285328-C-A

114336096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63285329-A-G

114336139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285372-T-C

http://identifiers.org/hco/9/GRCh38#114336314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285579-C-A

114336314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285579-C-T

http://identifiers.org/hco/9/GRCh38#114336355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285610-C-A

114336355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285610-C-T

114336502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285743-T-C

114336589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285848-T-C

http://identifiers.org/hco/9/GRCh38#114336648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285905-C-A

114336648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285905-C-G

114336673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285935-G-A

114336673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285935-G-T

http://identifiers.org/hco/9/GRCh38#114336676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63285938-C-A

114336676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285938-C-T

114336697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285959-C-T

114336698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63285960-A-G

114336786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286045-G-A

114336786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286045-G-C

114336786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286045-G-T

http://identifiers.org/hco/9/GRCh38#114336809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286067-C-A

http://identifiers.org/hco/9/GRCh38#114336818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286076-C-A

114336818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286076-C-T

http://identifiers.org/hco/9/GRCh38#114336823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286081-C-A

http://identifiers.org/hco/9/GRCh38#114336837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286095-C-A

http://identifiers.org/hco/9/GRCh38#114336845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286101-C-A

114336845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286101-C-T

114336871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286125-C-T

http://identifiers.org/hco/9/GRCh38#114336875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286129-C-A

114336875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286129-C-T

http://identifiers.org/hco/9/GRCh38#114336879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286133-C-A

114336879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286133-C-T

114336902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286158-A-G

114336902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286158-A-T

114336935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286186-A-G

114336971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286204-G-A

114336971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286204-G-C

114336971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286204-G-T

http://identifiers.org/hco/9/GRCh38#114337004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286245-A-C

114337004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286245-A-G

114337004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286245-A-T

http://identifiers.org/hco/9/GRCh38#114337035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286265-C-A

114337035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63286265-C-T

114337099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286328-G-A

114337099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286328-G-C

114337099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286328-G-T

114337123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286352-C-T

114337147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286376-G-A

114337210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286439-G-A

114337230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63286459-G-A

114337230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63286459-G-C

114337291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286508-T-A

114337291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286508-T-C

114337294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63286511-A-G

114337312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63286529-G-A

114337312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63286529-G-T

http://identifiers.org/hco/9/GRCh38#114337330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286547-C-A

114337330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63286547-C-G

114337330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63286547-C-T

http://identifiers.org/hco/9/GRCh38#114337385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63286586-C-A

114337385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63286586-C-G

114337385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63286586-C-T

114339212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63286963-G-A

114339304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63287036-G-A

114339551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63287280-T-C

114339551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63287280-T-G

http://identifiers.org/hco/9/GRCh38#114339663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63287388-C-A

114339663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63287388-C-T

114340625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63287831-T-A

114340700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63287899-G-A

114340842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288011-T-C

114340916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288078-G-A

114341161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288312-T-A

114341213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288431-G-C

114341213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288431-G-T

114341516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288693-A-G

114341534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63288710-C-G

114341534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63288710-C-T

114341564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63288740-C-G

http://identifiers.org/hco/9/GRCh38#114341649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63288825-C-A

114341649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63288825-C-T

114341794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288951-G-A

114341794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288951-G-T

http://identifiers.org/hco/9/GRCh38#114341801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63288961-C-A

114341801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288961-C-T

http://identifiers.org/hco/9/GRCh38#114341809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63288969-C-A

114341809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63288969-C-T

http://identifiers.org/hco/9/GRCh38#114341898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63289048-C-A

http://identifiers.org/hco/9/GRCh38#114341976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63289094-C-A

114342016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63289136-G-A

114342210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289318-G-A

114342210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289318-G-C

114342210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289318-G-T

114342247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289345-G-C

114342247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289345-G-T

114342312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289402-G-A

114342396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289483-C-T

114342768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289727-G-A

114342769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289728-C-G

114342988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63289892-C-G

114343710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63290036-G-A

114343710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63290036-G-C

114343749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63290075-A-T

114343766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63290092-T-G

http://identifiers.org/hco/9/GRCh38#114343817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63290142-C-A

114343832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290158-T-C

114343877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290189-T-C

114343898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290210-G-A

114343898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290210-G-T

http://identifiers.org/hco/9/GRCh38#114343955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63290260-C-A

114343955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290260-C-T

114343988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290271-G-T

114344056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290329-C-G

114344107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290381-C-T

114344131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290407-T-A

114344131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290407-T-C

114344131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290407-T-G

114344132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290408-T-G

114344249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290501-G-T

http://identifiers.org/hco/9/GRCh38#114344268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63290519-C-A

114344268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290519-C-T

114344323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290571-G-A

http://identifiers.org/hco/9/GRCh38#114344368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63290596-C-A

114344369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290597-T-A

114344369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290597-T-C

114344369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63290597-T-G

http://identifiers.org/hco/9/GRCh38#114344400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63290628-A-C

http://identifiers.org/hco/9/GRCh38#114344769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292381-C-A

114344775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63292375-A-G

114344775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63292375-A-T

114344817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63292329-G-A

114344817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63292329-G-T

http://identifiers.org/hco/9/GRCh38#114344819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292327-C-A

114344819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63292327-C-G

114344819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63292327-C-T

http://identifiers.org/hco/9/GRCh38#114345876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63291573-C-A

114345876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63291573-C-T

114345897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63291594-C-G

114345941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 63291638-G-A

114345942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63291639-T-C

114345944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63291641-G-A

114346099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63291771-G-T

http://identifiers.org/hco/9/GRCh38#114346107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63291777-C-A

114346107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63291777-C-G

114346107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63291777-C-T

114346110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63291780-G-A

114346110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63291780-G-T

114346542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292115-C-T

http://identifiers.org/hco/9/GRCh38#114346543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292116-C-A

114346543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292116-C-T

114346604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292164-G-A

114346604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292164-G-T

114346629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292187-T-C

114346638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292196-T-C

114346700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63292265-T-C

114346700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63292265-T-G

http://identifiers.org/hco/9/GRCh38#114346762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292327-C-A

114346762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292327-C-T

114346764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292329-G-A

114346808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292375-T-C

114346814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292381-T-A

114346814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292381-T-C

114346826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292393-T-C

114347606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292490-A-G

114347606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292490-A-T

114347608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292492-T-A

114347608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292492-T-G

114347627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292512-T-C

114347649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292532-G-A

114347692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292560-A-G

114347693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292561-G-A

114347702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292570-T-A

114347702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292570-T-G

114347795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63292662-G-C

114347795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63292662-G-T

114347833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 63292700-G-A

114347833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292700-G-C

114347833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292700-G-T

114347844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292711-T-C

http://identifiers.org/hco/9/GRCh38#114347865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292732-C-A

114347865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292732-C-T

114347870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63292737-C-T

http://identifiers.org/hco/9/GRCh38#114347896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292763-C-A

114347896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292763-C-G

114347896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63292763-C-T

114347911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292777-A-G

114347926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292791-A-G

114347957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292822-G-T

114347962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292827-C-T

114347964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292829-G-A

114347964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292829-G-C

114347964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292829-G-T

114347988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292853-T-G

http://identifiers.org/hco/9/GRCh38#114348027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63292885-C-A

114348027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292885-C-G

114348083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63292908-T-C

114348333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63293183-T-C

114348502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63293325-A-G

114348727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63293517-A-G

http://identifiers.org/hco/9/GRCh38#114348737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63293527-C-A

114348737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63293527-C-T

http://identifiers.org/hco/9/GRCh38#114348755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63293543-C-A

114348755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63293543-C-T

114349115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63293847-G-T

114349153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63293875-G-A

114349153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63293875-G-T

114349332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63294045-A-T

114349396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63294099-C-T

114349440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63294153-C-T

114349467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63294183-C-G

114349467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63294183-C-T

114350670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63294889-C-T

114350738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63294955-G-A

114350738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63294955-G-T

114350744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63294961-A-G

http://identifiers.org/hco/9/GRCh38#114350833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63295047-C-A

114350833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63295047-C-T

114350912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63295121-G-A

114350912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63295121-G-T

114350933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63295142-G-A

114355806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63295764-A-G

114355806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63295764-A-T

114355819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63295777-G-A

114355819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63295777-G-T

114355849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63295807-C-T

114355975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63295940-C-G

114355975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63295940-C-T

114356000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63295961-G-C

114356075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63296036-G-A

114356075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63296036-G-C

114356120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63296081-C-T

114356173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296131-C-T

114356198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296149-G-T

http://identifiers.org/hco/9/GRCh38#114356236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63296186-C-A

114356236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296186-C-T

http://identifiers.org/hco/9/GRCh38#114356254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63296203-A-C

114356254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296203-A-G

114356298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296252-G-A

114356514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296475-C-T

114356576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296541-G-A

114356737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296709-G-A

114356737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296709-G-T

114356898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63296842-G-A

114356987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296930-C-T

114357047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296989-G-A

114357047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296989-G-C

114357047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63296989-G-T

114357830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63297298-A-G

114357884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63297360-T-C

114357935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63297406-C-T

114357952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63297423-G-C

114357981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63297452-G-A

114357981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63297452-G-T

http://identifiers.org/hco/9/GRCh38#114358290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63297732-C-A

114358290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63297732-C-T

http://identifiers.org/hco/9/GRCh38#114358322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63297761-C-A

114358322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63297761-C-G

114358335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63297772-A-T

http://identifiers.org/hco/9/GRCh38#114359525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63298066-C-A

114359653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63298184-G-A

114359658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63298189-C-T

114359821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298352-G-A

114359844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298373-C-T

114359992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63298529-C-T

114360005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63298542-C-T

114360051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63298588-G-A

114360051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63298588-G-C

114360061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63298598-G-A

114360061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63298598-G-C

114360154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298673-T-A

114360154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298673-T-C

114360160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298679-G-C

114360160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298679-G-T

114360282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298801-A-G

114360282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298801-A-T

114360349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298853-A-T

114360576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298994-T-C

114360580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63298998-C-G

114360619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299032-A-G

114360693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299075-C-G

http://identifiers.org/hco/9/GRCh38#114360763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63299142-A-C

114360770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299149-T-C

114360788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299167-C-T

114360888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299253-G-A

114361110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299489-A-G

114361157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299528-G-A

114361307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299634-T-C

114361480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299794-T-C

114361647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63299908-T-C

http://identifiers.org/hco/9/GRCh38#114361739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63299997-C-A

114361740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63299998-T-A

114361863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63300118-C-T

114361875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63300130-G-A

114361875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63300130-G-C

114362002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300220-G-T

114362016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300233-G-T

114362037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300241-T-C

114362037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300241-T-G

114362044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300248-T-C

114362047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300251-T-A

114362047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300251-T-C

114362084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300284-T-C

114362178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300377-C-G

http://identifiers.org/hco/9/GRCh38#114362256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63300456-C-A

114362256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300456-C-G

114362256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300456-C-T

114362389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300563-T-C

114362419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63300593-A-G

114362475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63300649-C-T

114362530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63300704-A-G

http://identifiers.org/hco/9/GRCh38#114362558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63300728-A-C

114362607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300774-G-A

114362607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300774-G-T

114362628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300796-T-C

http://identifiers.org/hco/9/GRCh38#114362638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63300806-C-A

http://identifiers.org/hco/9/GRCh38#114362791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63300918-C-A

114362791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300918-C-T

http://identifiers.org/hco/9/GRCh38#114362868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63300980-C-A

114362887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300998-C-G

114362887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63300998-C-T

114363208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301300-G-A

114363256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301349-A-G

114364135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301721-T-C

114364213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301784-T-C

114364272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301844-G-T

114364375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301939-T-C

114364387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63301951-G-A

114364451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302016-G-A

114364451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302016-G-T

http://identifiers.org/hco/9/GRCh38#114364488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63302052-C-A

114364488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302052-C-T

114364533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302094-A-G

114364590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63302154-T-A

114364590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63302154-T-C

114364608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63302172-A-G

114364644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302207-T-C

http://identifiers.org/hco/9/GRCh38#114364695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63302262-C-A

114364695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302262-C-T

http://identifiers.org/hco/9/GRCh38#114364720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63302287-C-A

114364720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302287-C-T

114364733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302300-G-A

114364733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302300-G-C

114364733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302300-G-T

114364734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302301-G-A

114364734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302301-G-T

http://identifiers.org/hco/9/GRCh38#114364738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63302305-C-A

114364738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302305-C-T

114364946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302467-G-A

114365026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63302543-T-C

114366844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63304055-G-A

114367009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63304228-T-C

114367102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304317-T-C

http://identifiers.org/hco/9/GRCh38#114367627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63304551-C-A

114367627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63304551-C-T

114367659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63304583-G-A

http://identifiers.org/hco/9/GRCh38#114367660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63304584-C-A

114367660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63304584-C-G

114367660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63304584-C-T

114367675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63304599-G-C

114367675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63304599-G-T

114367712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304636-T-A

114367712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304636-T-G

114367713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304637-G-A

114367713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304637-G-T

114367726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304650-G-T

http://identifiers.org/hco/9/GRCh38#114367743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63304671-C-A

114367743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304671-C-T

http://identifiers.org/hco/9/GRCh38#114367763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63304693-C-A

http://identifiers.org/hco/9/GRCh38#114367809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63304728-A-C

114367809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304728-A-G

114367816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304735-G-A

114367816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304735-G-T

114367964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304881-G-C

114367997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63304914-G-A

114368086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305020-A-G

http://identifiers.org/hco/9/GRCh38#114368101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63305035-A-C

114368101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305035-A-G

http://identifiers.org/hco/9/GRCh38#114368199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63305107-C-A

114368199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 63305107-C-G

114368199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 63305107-C-T

114368406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305200-A-G

114368406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305200-A-T

http://identifiers.org/hco/9/GRCh38#114368411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63305207-C-A

114368411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305207-C-T

114368504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63305299-G-A

114368504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63305299-G-T

http://identifiers.org/hco/9/GRCh38#114368548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63305343-C-A

114368548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63305343-C-G

114368548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63305343-C-T

114368662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305461-T-C

114368668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305497-T-C

114368692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305520-T-C

http://identifiers.org/hco/9/GRCh38#114368706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63305534-C-A

http://identifiers.org/hco/9/GRCh38#114368724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63305551-C-A

114368724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305551-C-T

114368744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305561-G-A

114368744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305561-G-T

114368923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63305996-C-T

114369111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63306251-A-G

114369518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63306598-T-G

http://identifiers.org/hco/9/GRCh38#114369999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63307273-C-A

114370345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63307605-G-A

114370722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63307906-A-G

http://identifiers.org/hco/9/GRCh38#114370897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63308057-A-C

114370897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63308057-A-T

114370975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63308131-G-T

114371035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63308182-C-T

114371086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63308226-T-C

114372932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63309462-G-T

114373072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63309575-C-T

http://identifiers.org/hco/9/GRCh38#114373112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#63309641-C-A

114373112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63309641-C-T

114373240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63309775-A-G

114373288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63309816-G-T

http://identifiers.org/hco/9/GRCh38#114373320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63309866-C-A

114373414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63309971-T-G

114373535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63310052-G-A

114373535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63310052-G-T

114373580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310102-T-C

114373944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310181-A-T

114374001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310236-G-T

http://identifiers.org/hco/9/GRCh38#114374009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63310244-C-A

114374009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310244-C-T

http://identifiers.org/hco/9/GRCh38#114374042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63310294-C-A

114374042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310294-C-G

114374044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310296-C-T

http://identifiers.org/hco/9/GRCh38#114374085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63310348-C-A

114374085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63310348-C-T

114374096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63310372-G-T

114374117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63310393-A-G

114374117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63310393-A-T

114374170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63310446-G-A

114374170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63310446-G-T

114374188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310469-A-G

114374189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310470-C-T

114374197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310478-T-A

114374197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63310478-T-C

114375130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63311857-A-G

114375130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63311857-A-T

114375295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312019-T-C

http://identifiers.org/hco/9/GRCh38#114375304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63312028-C-A

114375304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312028-C-T

114375460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312148-G-A

114375504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312175-G-A

114375564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312203-T-C

114375725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312346-T-C

114375736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312357-G-A

http://identifiers.org/hco/9/GRCh38#114375971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63312470-C-A

114375971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312470-C-T

114375982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312481-T-A

114375982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312481-T-C

http://identifiers.org/hco/9/GRCh38#114376388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63312773-C-A

114376388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312773-C-T

114376440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312803-C-T

114376450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63312807-C-T

114376574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63312931-A-G

114376884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313241-G-A

114376935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313292-T-A

114376935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313292-T-C

114376988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63313345-C-T

114377031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313388-G-C

114377090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63313447-G-A

114377091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313448-G-A

114377118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313475-G-A

114377118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313475-G-T

114377195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63313552-C-T

114377324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313681-C-T

114377342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63313699-A-G

114377342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313699-A-T

http://identifiers.org/hco/9/GRCh38#114377378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63313717-C-A

114377378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63313717-C-T

114377450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63313789-G-A

114377500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63313839-T-A

114377543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 63313882-A-G

114377600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63313936-G-A

114377600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63313936-G-C

114377600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63313936-G-T

114377622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63313943-C-G

114377622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63313943-C-T

http://identifiers.org/hco/9/GRCh38#114377755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63314059-C-A

http://identifiers.org/hco/9/GRCh38#114377760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63314064-C-A

114377856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63314152-C-T

114377889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63314183-A-G

114378355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63314486-T-C

114378978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63314893-C-T

114379025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63314940-C-T

http://identifiers.org/hco/9/GRCh38#114379100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63315029-C-A

114379211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63315080-T-A

114379718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63315658-A-G

114381016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316069-T-A

114381016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316069-T-C

114381046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316099-G-A

http://identifiers.org/hco/9/GRCh38#114381051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63316104-C-A

114381051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316104-C-T

114381204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63316234-C-T

114381269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63316297-C-T

114381318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63316346-T-C

http://identifiers.org/hco/9/GRCh38#114381431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63316461-C-A

114381431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63316461-C-T

114381502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316525-T-A

114381502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316525-T-C

114381515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316534-T-C

http://identifiers.org/hco/9/GRCh38#114381518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63316537-C-A

114381518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316537-C-T

114381525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316544-G-C

114381528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316547-C-T

114381586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316582-G-C

114381586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316582-G-T

114381587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63316583-G-T

114382753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317212-T-A

114382917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317371-A-T

114383006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317446-A-G

114383017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63317482-G-A

114383017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63317482-G-C

114383017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63317482-G-T

114383021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63317492-G-T

http://identifiers.org/hco/9/GRCh38#114383307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63317751-C-A

114383438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317866-G-C

114383438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317866-G-T

114383580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317969-G-A

114383594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63317983-C-T

114385218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319141-C-T

114385277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63319181-G-A

114385277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63319181-G-C

114385277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63319181-G-T

114385334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319234-C-T

114385741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319612-C-T

114385847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63319718-C-T

114386101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319891-C-G

114386146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63319911-T-C

114386274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319983-G-A

114386274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319983-G-C

114386274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319983-G-T

114386285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63319993-C-T

114386297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63320005-G-A

114386445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63320151-G-C

114386517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63320209-C-G

114386863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63320610-C-T

114387288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63320970-C-G

114387288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63320970-C-T

114387630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321249-C-G

114387692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321289-G-A

114387695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321292-C-T

http://identifiers.org/hco/9/GRCh38#114387822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63321414-A-C

114387822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321414-A-G

114387822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321414-A-T

http://identifiers.org/hco/9/GRCh38#114387849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63321445-C-A

114387849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321445-C-T

114387887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63321483-C-T

114387986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 63321582-A-G

114388016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63321615-G-A

114388016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63321615-G-C

http://identifiers.org/hco/9/GRCh38#114388023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#63321622-A-C

114388023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 63321622-A-G

114388023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 63321622-A-T

114388051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63321647-G-A

114388051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63321647-G-T

114388074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63321680-G-A

114388074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63321680-G-T

http://identifiers.org/hco/9/GRCh38#114388080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63321686-C-A

114388080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63321686-C-G

114388162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63321764-A-G

114388183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63321781-C-T

114388299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321881-C-G

114388355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63321966-T-C

114388456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63322077-C-T

114388485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63322111-C-T

114388773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63322342-C-T

114389213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63322764-G-A

114389222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63322806-C-T

114389365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63322945-T-G

http://identifiers.org/hco/9/GRCh38#114389605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63323193-C-A

114389605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323193-C-T

114389608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323196-G-A

114389689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323262-A-G

114389704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323277-C-T

114389851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323367-C-T

114389885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323402-T-C

http://identifiers.org/hco/9/GRCh38#114389938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63323455-C-A

114389938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323455-C-T

114389944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323461-G-C

114390106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63323615-A-G

114390143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323632-A-G

114390263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63323735-C-T

114390326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63323790-G-A

114392541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63324817-G-A

114392549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63324825-G-A

114392566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63324842-T-C

114392628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63324906-T-C

114392957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63325212-A-T

114393155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63325447-T-C

114394442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63326180-T-C

114394461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63326197-T-C

http://identifiers.org/hco/9/GRCh38#114394486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63326222-C-A

114394801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63326487-G-C

114394809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron variant
orthologous variants: 63326495-G-C

114396701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: intron_variant, undefined
orthologous variants: 63327373-G-T

http://identifiers.org/hco/9/GRCh38#114396725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24108
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63327397-C-A