44285877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879480-G-A

44285877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879480-G-C

44285877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879480-G-T

44285971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77879402-G-A

44285971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77879402-G-T

http://identifiers.org/hco/21/GRCh38#44285980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77879393-C-A

44285980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77879393-C-G

44285980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77879393-C-T

http://identifiers.org/hco/21/GRCh38#44285995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#77879378-C-A

44285995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879378-C-T

http://identifiers.org/hco/21/GRCh38#44286000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#77879373-C-A

44286000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879373-C-T

http://identifiers.org/hco/21/GRCh38#44286020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77879339-C-A

44286020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77879339-C-T

44286061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77879298-G-A

44286061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77879298-G-T

44286103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879256-G-A

44286103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77879256-G-T

44286223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77879176-C-G

44286223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77879176-C-T

44286371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77879040-C-T

44286527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878936-G-A

44286527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878936-G-T

http://identifiers.org/hco/21/GRCh38#44286809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77878680-C-A

44286809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878680-C-G

44286809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878680-C-T

44287221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878272-C-T

44287236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878265-G-A

44287236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878265-G-C

44287256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878247-G-A

44287256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878247-G-C

44287256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878247-G-T

http://identifiers.org/hco/21/GRCh38#44287329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77878164-C-A

44287372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878124-T-C

44287403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878081-G-A

44287403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878081-G-C

http://identifiers.org/hco/21/GRCh38#44287450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77878029-C-A

44287450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878029-C-T

44287454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878027-T-C

http://identifiers.org/hco/21/GRCh38#44287460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77878021-C-A

44287460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878021-C-G

44287460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878021-C-T

http://identifiers.org/hco/21/GRCh38#44287461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77878020-C-A

44287461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878020-C-G

44287461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77878020-C-T

44287487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77877997-G-A

44287487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77877997-G-T

http://identifiers.org/hco/21/GRCh38#44287537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77877947-C-A

44287537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877947-C-G

44287537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877947-C-T

44287588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877896-A-G

44287588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877896-A-T

44287946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877637-C-T

44288138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877491-T-A

44288383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877407-G-A

44288419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877371-G-A

44288419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77877371-G-T

44288490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877307-G-T

44288540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877279-T-A

44288540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877279-T-C

http://identifiers.org/hco/21/GRCh38#44288587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77877227-C-A

http://identifiers.org/hco/21/GRCh38#44288591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77877223-C-A

44288591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877223-C-T

http://identifiers.org/hco/21/GRCh38#44288626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77877189-C-A

44288626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877189-C-T

44288632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877183-A-G

44288644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877169-G-A

44288644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877169-G-T

http://identifiers.org/hco/21/GRCh38#44288722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77877107-C-A

44288756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877075-A-G

44288782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877054-C-T

http://identifiers.org/hco/21/GRCh38#44288823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77877015-C-A

44288867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876950-A-G

http://identifiers.org/hco/21/GRCh38#44288882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876937-C-A

44288882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876937-C-T

44289012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876815-C-T

44289016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876811-G-A

44289016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876811-G-T

44289025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876802-G-T

44289133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876689-G-T

44289153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876671-T-C

44289183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876641-T-C

http://identifiers.org/hco/21/GRCh38#44289186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876638-C-A

44289186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876638-C-T

44289187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876637-T-C

44289187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876637-T-G

http://identifiers.org/hco/21/GRCh38#44289188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876636-C-A

http://identifiers.org/hco/21/GRCh38#44289210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876616-C-A

44289210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876616-C-G

44289210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876616-C-T

http://identifiers.org/hco/21/GRCh38#44289292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876549-C-A

44289292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77876549-C-G

44289292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77876549-C-T

44289384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77876461-A-T

44289393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77876452-C-T

44289404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77876412-A-T

44289437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876375-T-C

44289437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876375-T-G

http://identifiers.org/hco/21/GRCh38#44289438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876374-C-A

44289438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876374-C-T

http://identifiers.org/hco/21/GRCh38#44289446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876361-A-C

44289446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876361-A-G

44289446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876361-A-T

44289459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876348-G-A

44289459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876348-G-C

44289459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876348-G-T

44289497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876220-T-A

44289497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876220-T-C

http://identifiers.org/hco/21/GRCh38#44289516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876186-A-C

44289516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876186-A-G

44289516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876186-A-T

44289524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876178-G-C

44289524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876178-G-T

44289543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876159-G-A

44289543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77876159-G-T

http://identifiers.org/hco/21/GRCh38#44289577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876098-C-A

http://identifiers.org/hco/21/GRCh38#44289578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77876097-C-A

44289652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77875916-C-T

44289887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875668-C-G

44289887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875668-C-T

http://identifiers.org/hco/21/GRCh38#44289961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77875602-C-A

http://identifiers.org/hco/21/GRCh38#44289962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77875601-A-C

44289962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875601-A-G

44291267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873664-C-T

44291297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873638-G-A

44291297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873638-G-T

44291377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873549-G-A

44291560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873397-T-A

44292023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77872968-G-T

44292152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77872781-T-C

http://identifiers.org/hco/21/GRCh38#44292197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77872739-C-A

http://identifiers.org/hco/21/GRCh38#44292295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77872623-C-A

44292295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77872623-C-T

http://identifiers.org/hco/21/GRCh38#44292377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77872541-C-A

44292377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77872541-C-G

44292377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77872541-C-T

44292383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77872535-G-A

44292383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77872535-G-T

http://identifiers.org/hco/21/GRCh38#44292388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77872530-C-A

44292388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77872530-C-T

http://identifiers.org/hco/21/GRCh38#44293035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871623-C-A

44293035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871623-C-T

http://identifiers.org/hco/21/GRCh38#44293046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871612-A-C

44293046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77871612-A-G

44293046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871612-A-T

http://identifiers.org/hco/21/GRCh38#44293048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871610-C-A

44293048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871610-C-G

44293048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871610-C-T

http://identifiers.org/hco/21/GRCh38#44293083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871575-C-A

44293083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871575-C-G

44293083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871575-C-T

http://identifiers.org/hco/21/GRCh38#44293099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871559-C-A

44293099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77871559-C-G

44293134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77871530-G-A

44293159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77871505-G-A

44293159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77871505-G-C

44293159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77871505-G-T

44293160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77871504-T-A

44293169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77871495-T-C

http://identifiers.org/hco/21/GRCh38#44293173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871491-C-A

44293173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 77871491-C-T

http://identifiers.org/hco/21/GRCh38#44293209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871445-C-A

44293209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871445-C-G

44293209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871445-C-T

44293213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871441-G-A

44293213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871441-G-C

44293213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871441-G-T

44293221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871433-G-A

44293221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871433-G-T

44293225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871429-T-A

44293225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871429-T-C

http://identifiers.org/hco/21/GRCh38#44293242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77871414-C-A

44293242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871414-C-T

http://identifiers.org/hco/21/GRCh38#44293831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77870497-A-C

44293831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77870497-A-G

44293885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77870443-T-C

44293894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77870434-G-A

44293894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77870434-G-C

44293894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77870434-G-T

44293942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77870381-A-G

44293944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77870379-C-T

http://identifiers.org/hco/21/GRCh38#44293954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77870369-A-C

44293954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77870369-A-G

44294402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 77870320-A-G

44294402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 77870320-A-T

44296241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867849-C-G

44296241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867849-C-T

http://identifiers.org/hco/21/GRCh38#44296299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77867800-C-A

44296307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867792-C-T

44296330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867773-C-T

44296338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867767-G-A

44296338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867767-G-C

http://identifiers.org/hco/21/GRCh38#44296398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77867700-C-A

44296451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867647-G-A

44296831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867430-G-A

44296831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867430-G-T

44297524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866271-G-A

44297524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866271-G-T

http://identifiers.org/hco/21/GRCh38#44297556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#77866242-A-C

44297556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77866242-A-G

44297556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77866242-A-T

http://identifiers.org/hco/21/GRCh38#44297601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77866202-C-A

44297601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866202-C-T

http://identifiers.org/hco/21/GRCh38#44297619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77866193-C-A

44297619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866193-C-G

44297619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866193-C-T

44297620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866192-G-A

44297620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866192-G-T

44297712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77866091-C-G

http://identifiers.org/hco/21/GRCh38#44297731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#77866072-C-A

44297731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77866072-C-T

http://identifiers.org/hco/21/GRCh38#44297739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#77866058-C-A

44297739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 360
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77866058-C-T