1666078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139894463-G-C

1666219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139894601-C-T

1666252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139894634-C-T

1666464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139894856-G-A

1666464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139894856-G-C

1666506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139894891-C-G

1666722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139895091-C-G

1666859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139895209-C-T

1667212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139895539-C-T

1667326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139895665-C-T

1667415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139895731-A-T

1667473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139895791-A-G

http://identifiers.org/hco/7/GRCh38#1667766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139896094-C-A

1667787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896115-G-A

1667787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896115-G-T

1667857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896182-C-T

1667944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896284-C-T

1667964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896296-G-A

1667964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896296-G-T

1668003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896340-G-T

1668019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896357-A-G

http://identifiers.org/hco/7/GRCh38#1668539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139896839-C-A

1668629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896887-T-A

1668629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896887-T-G

1668633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139896891-G-T

1668962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897111-C-G

1669027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897176-C-T

1669057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897209-C-G

1669095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897247-C-G

1669095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897247-C-T

1669117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897269-C-G

http://identifiers.org/hco/7/GRCh38#1669187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139897353-C-A

1669716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897863-C-G

1669716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897863-C-T

http://identifiers.org/hco/7/GRCh38#1669860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139897995-A-C

1669860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897995-A-G

1669860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139897995-A-T

1670004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139898075-C-G

1670124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139898187-G-T

1670205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139898258-T-C

1670205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139898258-T-G

1670206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139898262-T-C

1670317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898401-C-G

1670317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898401-C-T

1670324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898408-C-G

1670757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898833-T-A

1670777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898856-G-A

1670777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898856-G-C

1670845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898908-C-G

1670900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139898963-C-T

1671135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899150-T-G

http://identifiers.org/hco/7/GRCh38#1671160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139899174-A-C

1671160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899174-A-G

1671189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899204-C-T

1671294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899319-G-A

1671534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899537-G-T

1671641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899616-C-T

1671666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899641-T-C

1671916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899835-G-A

1671988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899912-G-T

1671994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899918-C-T

1672041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139899967-C-T

1672113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139900023-C-T

1672406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900252-G-T

1672553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900377-T-C

1672737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900581-C-G

1672737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900581-C-T

1673136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900959-A-G

1673583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901298-C-G

1673583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901298-C-T

1673601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901315-C-T

1673693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901380-C-T

1673932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901570-G-A

1673992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901622-C-G

1674070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901668-T-C

1674073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901671-T-C

1674132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901725-G-A

1674538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901921-G-A

1674538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901921-G-T

1674574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901953-G-A

1674694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902054-G-T

1674837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902184-G-A

http://identifiers.org/hco/7/GRCh38#1675058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139902364-A-C

1675058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902364-A-G

http://identifiers.org/hco/7/GRCh38#1675139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139902435-C-A

1677199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139904791-A-T

1677805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139905033-C-T

1677828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139905053-G-C

1677880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139905110-C-T

1677941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139905157-G-T

1678080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139905311-C-G

1678080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139905311-C-T

http://identifiers.org/hco/7/GRCh38#1690377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139914653-A-C

1690377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914653-A-G

1690380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914656-A-G

1690389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914665-G-A

1690405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914681-G-A

1690412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914688-A-G

1690424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914700-A-G

1690431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914707-G-A

1690440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914716-G-A

1690447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914728-G-C

1690449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914730-T-C

1690450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914731-G-C

1690459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914740-G-A

1690487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914768-G-A

1690495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914776-A-G

1690520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914801-G-A

1690596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139914877-A-G

1690902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139915186-C-T

1690965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139915237-T-C

1691004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139915271-A-G

1691194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139915431-G-C

1691623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139915775-C-T

1691706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139915860-G-A

http://identifiers.org/hco/7/GRCh38#1691762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139915912-C-A

1691882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139916041-G-T

1692062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916187-A-G

http://identifiers.org/hco/7/GRCh38#1692116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139916221-C-A

1692116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916221-C-T

1692429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916646-G-C

1692448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916669-T-C

1692448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916669-T-G

1692464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916688-T-C

1692465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916689-G-A

1692465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139916689-G-T

1692572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139916859-G-T

1692602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139916897-G-A

http://identifiers.org/hco/7/GRCh38#1692885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917210-C-A

1692885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917210-C-T

1692956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917251-T-C

1692969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917263-C-T

http://identifiers.org/hco/7/GRCh38#1693000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917293-C-A

1693000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917293-C-T

http://identifiers.org/hco/7/GRCh38#1693078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917390-C-A

http://identifiers.org/hco/7/GRCh38#1693083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917395-C-A

1693083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917395-C-G

1693083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917395-C-T

http://identifiers.org/hco/7/GRCh38#1693098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917409-C-A

1693098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917409-C-T

http://identifiers.org/hco/7/GRCh38#1693104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917415-C-A

1693104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917415-C-G

1693116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917426-G-A

1693116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917426-G-T

1693120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917433-A-G

1693120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917433-A-T

http://identifiers.org/hco/7/GRCh38#1693146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917458-C-A

1693146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917458-C-G

1693146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917458-C-T

1693155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917475-A-G

http://identifiers.org/hco/7/GRCh38#1693232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139917573-C-A

1693265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917605-A-G

1693282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917620-T-C

1693622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917819-G-A

1693753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139917984-G-A

http://identifiers.org/hco/7/GRCh38#1693832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139918048-C-A

1693832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918048-C-T

1693855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918071-G-A

1693855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918071-G-C

1693857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918073-T-A

1693963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918118-G-A

1693963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918118-G-T

1693983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918131-C-T

http://identifiers.org/hco/7/GRCh38#1694073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139918206-C-A

1694191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918320-G-A

1694191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918320-G-T

http://identifiers.org/hco/7/GRCh38#1694206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139918344-C-A

1694211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918349-T-C

1694216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918354-G-T

1694271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139918403-A-T

1694366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139918485-G-A

1694366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139918485-G-T

1694556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139918656-G-A

1694571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139918671-G-A

1694628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139918714-G-A

1698416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139921294-T-C

1698423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139921298-C-T

1702771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139925925-G-A

1702860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139926014-C-T

1703029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139926300-C-T

1703337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139926826-C-T

1703757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139927317-C-G

1703775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139927335-G-A

1704149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139929045-C-T

1704472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139929368-C-T

http://identifiers.org/hco/7/GRCh38#1704493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139929402-C-A

1704497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139929406-C-T

1705013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139930388-C-T

1705397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139930731-C-T

1705893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139931083-C-G

1705893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139931083-C-T

1707402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139931850-C-G

1707456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139931881-C-T

1707541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139931956-G-A

1707591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139931993-G-C

1707842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139932311-C-T

1707926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139932389-C-T

1708017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139932440-G-A

1710068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: 139933409-G-A

1710104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139933445-C-G

1710116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139933457-C-T

1710139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139933480-C-T

1711916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139933807-A-G

1713210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139934391-G-A

1713235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139934424-G-C

1713423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139934778-T-C

1713757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: 139935161-G-A

1713757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: 139935161-G-C

1713836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: 139935216-A-G

http://identifiers.org/hco/7/GRCh38#1714034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#139935374-C-A

1714034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: 139935374-C-T

1714035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, undefined
orthologous variants: 139935375-G-A

1714417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139935701-C-G

1714744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936083-A-G

1714844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936167-C-T

1714845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936168-G-A

1714845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936168-G-C

1714845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936168-G-T

1714916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936233-G-A

1715001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936310-G-A

1717110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139936937-C-T

1717291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139937088-C-T

1722656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139939579-T-C

1722671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139939594-T-C

1727469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139943292-G-A

1727519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139943343-C-T

1727611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139943415-G-A

1732358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139947294-C-T

1732450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139947381-T-C

1733914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139949702-T-A

1733914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139949702-T-C

1733976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139949764-A-T

1734270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139950029-C-T

1735342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139950672-G-A

1735444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139950765-T-C

1735564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139950854-C-G

1735623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139950912-C-G

1735801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951039-A-G

1735849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951092-G-T

1735851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951094-A-T

http://identifiers.org/hco/7/GRCh38#1736095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139951307-A-C

1736181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951392-A-G

1736265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951476-C-T

1736450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951642-C-T

1736493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951685-G-A

1736543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951729-G-A

1736590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139951780-G-A

http://identifiers.org/hco/7/GRCh38#1742192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139955053-C-A

1742252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139955113-G-A

1742868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139955441-C-T

1743014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139955584-A-G

1743420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139955975-C-T

1743468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956070-C-T

1743707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956236-G-A

1743802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956339-A-G

1743852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956386-C-T

1744114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956571-T-A

http://identifiers.org/hco/7/GRCh38#1744168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139956628-C-A

1744168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956628-C-T

http://identifiers.org/hco/7/GRCh38#1744191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139956653-C-A

1744191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956653-C-G

1744191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956653-C-T

http://identifiers.org/hco/7/GRCh38#1744259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139956694-C-A

1744259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956694-C-G

1744260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: intron variant
orthologous variants: 139956695-T-C

1744331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5 prime UTR variant
orthologous variants: 139956762-T-C

http://identifiers.org/hco/7/GRCh38#1744438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139956869-C-A

1744438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5 prime UTR variant
orthologous variants: 139956869-C-T

1744552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 5 prime UTR variant
orthologous variants: 139956976-T-C

http://identifiers.org/hco/7/GRCh38#1744632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957033-C-A

1744632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957033-C-T

1744713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957114-G-A

1744713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957114-G-T

http://identifiers.org/hco/7/GRCh38#1744743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957144-C-A

1744743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957144-C-T

http://identifiers.org/hco/7/GRCh38#1744818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957219-C-A

1744818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957219-C-T

1744821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957222-G-A

1744821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957222-G-T

http://identifiers.org/hco/7/GRCh38#1744827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957228-C-A

1744827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957228-C-T

http://identifiers.org/hco/7/GRCh38#1744893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957294-C-A

1744893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957294-C-G

1744893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957294-C-T

1744908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957309-C-T

1745145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957546-G-A

1745154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957555-G-T

1745209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957610-C-T

http://identifiers.org/hco/7/GRCh38#1745214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957615-C-A

1745214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957615-C-T

1745290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957691-C-G

1745290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957691-C-T

1745388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957792-T-C

1745402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957806-G-A

1745402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957806-G-C

1745402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957806-G-T

1745406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957810-A-G

1745412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957816-G-A

1745412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957816-G-C

1745412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957816-G-T

1745448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957849-C-T

1745463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139957864-T-G

http://identifiers.org/hco/7/GRCh38#1745496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139957897-C-A

1745496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139957897-C-T

1745610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958011-G-A

1745610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958011-G-C

1745610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958011-G-T

http://identifiers.org/hco/7/GRCh38#1745877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139958278-C-A

1745877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958278-C-T

http://identifiers.org/hco/7/GRCh38#1745907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#139958308-C-A

1745907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: stop gained
orthologous variants: 139958308-C-G

1745907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958308-C-T

1745976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958374-C-T

1746072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139958470-G-T

1746102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958500-G-A

1746102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958500-G-C

1746102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139958500-G-T

1746203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139958604-G-A

1746203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139958604-G-T

http://identifiers.org/hco/7/GRCh38#1746672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139959076-C-A

1746672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139959076-C-G

1746672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139959076-C-T

http://identifiers.org/hco/7/GRCh38#1746696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#139959100-C-A

1746696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: stop gained
orthologous variants: 139959100-C-G

1746696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: 139959100-C-T

http://identifiers.org/hco/7/GRCh38#1746820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139959221-C-A

1746820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139959221-C-G

1746820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: missense variant
orthologous variants: 139959221-C-T

http://identifiers.org/hco/7/GRCh38#1747104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139959550-C-A

1747104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959550-C-T

1747130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959576-T-A

http://identifiers.org/hco/7/GRCh38#1747180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139959641-A-C

1747180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959641-A-G

1747232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959695-A-G

1747293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959760-G-A

1747293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959760-G-T

1747367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959977-G-A

1747367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959977-G-C

1747367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959977-G-T

1747373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959983-T-A

1747373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959983-T-C

1747373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959983-T-G

1747374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959984-G-A

1747374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959984-G-C

1747374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959984-G-T

1747387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139959996-T-A

http://identifiers.org/hco/7/GRCh38#1747400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139960009-C-A

1747400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139960009-C-G

1747400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139960009-C-T

1747501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139960108-G-C

1747501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139960108-G-T

1747767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33154
most severe consequence: 3 prime UTR variant
orthologous variants: 139960319-C-T