44066703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 93679813-T-G

http://identifiers.org/hco/11/GRCh38#44066783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679740-C-A

44066783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93679740-C-T

44066798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93679725-T-A

44066798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93679725-T-C

http://identifiers.org/hco/11/GRCh38#44066843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679676-A-C

http://identifiers.org/hco/11/GRCh38#44066965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679568-A-C

44067021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93679522-G-T

44067130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93679430-T-C

http://identifiers.org/hco/11/GRCh38#44067205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679369-C-A

44067205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93679369-C-T

http://identifiers.org/hco/11/GRCh38#44067212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679363-C-A

http://identifiers.org/hco/11/GRCh38#44067264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679322-C-A

44067264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 93679322-C-T

44067279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93679310-T-C

44067326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679263-G-T

44067365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679223-A-T

http://identifiers.org/hco/11/GRCh38#44067367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679221-A-C

http://identifiers.org/hco/11/GRCh38#44067373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679215-C-A

44067373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679215-C-T

http://identifiers.org/hco/11/GRCh38#44067425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93679165-C-A

44067425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679165-C-T

44067487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679115-G-T

44067522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679085-G-A

44067587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678590-G-T

44067590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678587-A-G

http://identifiers.org/hco/11/GRCh38#44067633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93678545-C-A

44067633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93678545-C-T

44067700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93678478-G-A

44067700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93678478-G-C

44067748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93678430-G-A

44067748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93678430-G-T

44067790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93678385-A-G

44067801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93678374-T-C

http://identifiers.org/hco/11/GRCh38#44067810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93678365-C-A

44067810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93678365-C-T

44067920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678255-G-A

44068009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678185-A-G

44068009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678185-A-T

44068012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678182-A-T

44068043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678152-A-G

44068043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93678152-A-T

http://identifiers.org/hco/11/GRCh38#44069075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93677654-A-C

44069433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93677542-T-C

44069877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93677195-G-T

44070058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93677066-G-C

44070119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93677028-G-A

44070295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93676876-A-G

http://identifiers.org/hco/11/GRCh38#44070547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93676700-C-A

44070547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93676700-C-T

44070600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93676670-C-G

44070707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93676612-T-A

44071236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93676167-T-C

44071256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 93676149-G-A

44071298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93676107-G-C

44071331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93676028-C-G

44071331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93676028-C-T

44071385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93675929-A-G

44071395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93675919-T-G

44071417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93675897-G-A

44072738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675283-A-T

44072856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675178-G-C

44072866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675168-C-T

44073078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674958-C-T

44073530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93674533-C-T

44073598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93674449-G-A

44073598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93674449-G-T

44073632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674432-G-A

44073632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674432-G-T

http://identifiers.org/hco/11/GRCh38#44073660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93674405-A-C

44073660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674405-A-G

http://identifiers.org/hco/11/GRCh38#44073670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93674395-C-A

44073670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674395-C-T

44073672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674393-G-A

44073672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674393-G-T

44073683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674383-G-A

44073683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674383-G-T

44073753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674293-G-C

44073855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674208-T-C

44073902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674173-G-A

44073902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674173-G-T

44074454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673483-G-A

44074465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673476-A-G

http://identifiers.org/hco/11/GRCh38#44074490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93673457-C-A

44074490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673457-C-T

http://identifiers.org/hco/11/GRCh38#44074491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93673456-C-A

44074491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673456-C-T

44074494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673453-A-G

http://identifiers.org/hco/11/GRCh38#44074529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93673414-C-A

44074536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673407-T-C

44074625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93673318-G-T

44075245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673199-T-G

44075265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673179-A-G

44075304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673139-G-A

44075518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93672966-G-A

44075519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93672965-C-T

44075597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672887-G-A

44077135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672446-G-T

44077141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672440-T-G

44077163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672418-G-A

44077163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672418-G-T

http://identifiers.org/hco/11/GRCh38#44077165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93672416-C-A

44077165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672416-C-T

44077201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672380-G-A

44077201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93672380-G-T

http://identifiers.org/hco/11/GRCh38#44077272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93672312-C-A

44077272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93672312-C-T

44077293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672291-C-G

44077296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672288-A-G

44077398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672198-G-A

44077464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672120-G-A

44077464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672120-G-T

44077465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672119-G-T

44077514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672070-G-A

44077514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672070-G-T

http://identifiers.org/hco/11/GRCh38#44077515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93672069-C-A

44077515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672069-C-T

44077539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 93672045-G-A

http://identifiers.org/hco/11/GRCh38#44077597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93671990-C-A

44077597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671990-C-G

44077597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671990-C-T

http://identifiers.org/hco/11/GRCh38#44077630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93671958-A-C

44077630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671958-A-G

http://identifiers.org/hco/11/GRCh38#44077696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93671875-A-C

44077696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671875-A-G

44077696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671875-A-T

44077734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671838-C-T

44077769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671803-G-A

44077769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671803-G-T

http://identifiers.org/hco/11/GRCh38#44077863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93671711-C-A

44077863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93671711-C-G

44077863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93671711-C-T

44077879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93671695-C-G

44077967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671608-G-A

44078013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671577-G-A

44078013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671577-G-T

44078057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671537-G-A

44078057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671537-G-T

44078128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671458-G-T

44078139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671447-A-G

44078139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671447-A-T

44078156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671434-G-T

44078157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93671433-A-G

44078244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670888-A-G

44078344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670799-G-C

44078344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670799-G-T

http://identifiers.org/hco/11/GRCh38#44078354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93670791-C-A

44078354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670791-C-G

http://identifiers.org/hco/11/GRCh38#44078415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93670726-A-C

44078415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670726-A-G

44078449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670705-A-G

44078449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670705-A-T

http://identifiers.org/hco/11/GRCh38#44078450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93670704-C-A

44078450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670704-C-G

44078450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670704-C-T

44078520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670625-G-A

44078520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670625-G-T

44078586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670559-A-G

44078608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670544-G-A

44078608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670544-G-C

44078608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670544-G-T

http://identifiers.org/hco/11/GRCh38#44078615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93670537-C-A

44078648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670494-G-A

44078648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670494-G-T

http://identifiers.org/hco/11/GRCh38#44078659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93670483-C-A

44078659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670483-C-T

44078802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93670356-G-A

44079221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669853-G-T

http://identifiers.org/hco/11/GRCh38#44079284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93669809-A-C

44079284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669809-A-G

44079284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669809-A-T

44079324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669769-T-A

44079324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669769-T-C

http://identifiers.org/hco/11/GRCh38#44079340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93669753-C-A

44079340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669753-C-T

http://identifiers.org/hco/11/GRCh38#44079407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93669697-C-A

44079408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669696-A-T

44079509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669602-C-T

44079670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669440-A-G

http://identifiers.org/hco/11/GRCh38#44079691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93669419-C-A

44079691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669419-C-G

44079691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669419-C-T

44079701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669409-G-T

44079704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669406-A-G

http://identifiers.org/hco/11/GRCh38#44079708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93669402-C-A

44079708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669402-C-T

http://identifiers.org/hco/11/GRCh38#44079709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93669401-C-A

44079709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669401-C-T

44079778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669342-G-A

44079858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669265-T-C

44079872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669251-A-G

44079965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669162-C-T

44080589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669059-G-T

44080597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669052-A-G

44080610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669039-A-G

http://identifiers.org/hco/11/GRCh38#44080651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93668998-A-C

44080651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668998-A-G

44080689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668961-A-G

44080689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668961-A-T

44080755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668898-G-T

44080788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668806-T-A

44080788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668806-T-C

http://identifiers.org/hco/11/GRCh38#44080852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93668764-C-A

44080852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668764-C-T

http://identifiers.org/hco/11/GRCh38#44080870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93668748-A-C

44080870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668748-A-G

44080928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668714-T-G

44081007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668641-G-A

http://identifiers.org/hco/11/GRCh38#44081153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93668521-A-C

44081153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93668521-A-G

44081200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93668474-C-T

http://identifiers.org/hco/11/GRCh38#44081382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93668294-C-A

44081382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668294-C-G

44081391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668285-A-G

http://identifiers.org/hco/11/GRCh38#44081439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93668239-C-A

44081439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668239-C-T

44081453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668225-G-A

44081453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668225-G-T

44081506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668179-A-G

44081522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668171-G-A

44081616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93668090-G-A

44081790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667959-A-G

44081790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667959-A-T

44081831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667911-T-A

44081843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667899-A-G

44082119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93667639-T-A

44082130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93667628-A-T

44082139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93667619-A-T

44082161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93667600-A-T

44082296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667490-G-C

44082572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667262-G-A

44082616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667241-A-G

44082734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667126-T-C

44082800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667012-C-T

44082816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666994-A-G

44082840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666970-G-T

44082928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666881-G-T

http://identifiers.org/hco/11/GRCh38#44083016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93666808-C-A

44083028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666796-T-A

44083062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666769-A-G

44083079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666753-T-A

44083080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666752-G-C

http://identifiers.org/hco/11/GRCh38#44083124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93666709-A-C

44083124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666709-A-G

44083135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666698-G-A

44083240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93666602-G-C

44083254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93666588-G-A

44083384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666464-G-A

44083458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93666392-T-C

44083550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93666300-T-G

44083677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93666189-C-T

44083688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93666178-T-A

44083769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93666097-G-A

44083769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93666097-G-C

44083833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93666053-G-T

44083857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93666026-G-A

44083931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93665952-T-A

44083931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93665952-T-C

44083942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93665941-T-A

44083942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93665941-T-C

44084061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93665826-G-A

44084061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93665826-G-T

44084227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23989
most severe consequence: 3 prime UTR variant
orthologous variants: 93665646-T-G