69709522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3 prime UTR variant
orthologous variants: 23706288-T-A

69709698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23706124-C-T

69709706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23706116-A-G

69709825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23706000-C-T

69710081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23705755-A-G

69710177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23705654-T-C

http://identifiers.org/hco/9/GRCh38#69710224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23705611-C-A

69710224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23705611-C-T

69710468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23705334-C-T

69710746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23705088-G-T

69710774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23705062-G-T

69710923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704944-G-C

69710940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704927-T-C

69710943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704924-C-T

69711085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704786-C-T

http://identifiers.org/hco/9/GRCh38#69711257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23704633-C-A

69711257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704633-C-T

69711331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704562-A-T

69711337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704556-C-G

69711348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704545-G-A

69711348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704545-G-T

69711602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23704324-T-C

69711965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703986-A-G

69712089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703861-A-G

69712101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703850-A-G

http://identifiers.org/hco/9/GRCh38#69712128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23703834-C-A

69712377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703607-G-A

69712490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703380-A-G

69712580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703296-A-G

69712673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703204-T-C

69712952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23703091-T-C

69713431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702620-T-C

69713553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702517-T-C

69713674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702336-G-A

69713696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702314-A-G

69713712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702297-T-C

69713741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702262-G-A

69713762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23702241-G-A

http://identifiers.org/hco/9/GRCh38#69714003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23702019-C-A

69714049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23701980-T-A

69714049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23701980-T-C

69714050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23701979-G-C

69714095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23701903-T-C

69714756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23701230-T-C

69714859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23701171-T-G

69715236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23700818-T-A

69715252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23700800-A-G

http://identifiers.org/hco/9/GRCh38#69715446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23700618-C-A

69715467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23700602-C-T

69715485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23700586-G-T

69715950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23700159-T-A

69715964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23700145-G-A

69716424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23699725-T-G

69716593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23699563-G-A

http://identifiers.org/hco/9/GRCh38#69716687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23699467-C-A

69716902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698980-G-T

69716935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698945-T-C

http://identifiers.org/hco/9/GRCh38#69717014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23698863-C-A

http://identifiers.org/hco/9/GRCh38#69717021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23698856-C-A

69717021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698856-C-T

http://identifiers.org/hco/9/GRCh38#69717026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23698849-C-A

http://identifiers.org/hco/9/GRCh38#69717085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23698797-A-C

http://identifiers.org/hco/9/GRCh38#69717173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23698683-C-A

69717173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698683-C-G

69717173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698683-C-T

69717379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698469-G-T

69717537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698295-T-C

69717668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698155-G-A

69718022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23698069-G-T

69718091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697995-G-A

69718091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697995-G-T

69718092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697994-G-C

69718202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697889-G-T

69718216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697875-T-C

69718216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697875-T-G

http://identifiers.org/hco/9/GRCh38#69718223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23697868-C-A

69718223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697868-C-G

69718223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23697868-C-T

http://identifiers.org/hco/9/GRCh38#69718385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23697719-A-C

69718385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23697719-A-T

69718399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23697705-C-T

69718655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23697449-A-G

69718958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23697184-T-C

69722030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696349-G-A

69722056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696323-T-A

69722253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23696140-C-G

69723047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695727-G-A

69723138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695649-A-G

69723216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695570-A-T

69723220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695566-G-T

http://identifiers.org/hco/9/GRCh38#69723248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23695538-C-A

69723248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695538-C-T

69723288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695503-G-A

69723288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23695503-G-T

69723430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23695360-T-G

69723477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23695328-C-T

69723506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23695299-G-A

69724568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694880-G-C

69724861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23694565-T-A

69727280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23691026-C-T

69727427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690914-G-C

http://identifiers.org/hco/9/GRCh38#69727519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23690823-A-C

69727519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690823-A-G

69727532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690810-C-G

69727823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690546-T-G

69727867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690526-G-T

http://identifiers.org/hco/9/GRCh38#69727972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23690399-A-C

69728155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690038-T-A

69728155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23690038-T-C

69728198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23689993-G-T

http://identifiers.org/hco/9/GRCh38#69728437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23689776-A-C

69728720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23689534-C-G

69729077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23689403-T-C

69729674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23688732-T-A

69729674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23688732-T-C

69730004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23688238-T-C

69730028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23688214-C-T

69730097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23688162-A-G

69730195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23688070-T-C

69730297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687988-C-T

69730325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687958-G-C

69730362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687921-T-C

69730682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687634-T-C

69730907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687427-C-T

69730962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687376-C-T

69731138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687213-T-A

69731339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23687046-C-G

69731415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23686968-C-T

69731532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23686843-C-T

http://identifiers.org/hco/9/GRCh38#69731801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23686617-C-A

69731801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23686617-C-T

http://identifiers.org/hco/9/GRCh38#69731805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23686613-C-A

69731948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23686490-C-G

69731948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23686490-C-T

69731958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23686480-G-C

69732004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23686434-G-T

http://identifiers.org/hco/9/GRCh38#69732036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23686402-C-A

69732036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23686402-C-T

69732091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23686372-T-C

69732472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23686010-T-C

69732594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23685116-C-T

69733290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23684442-T-C

http://identifiers.org/hco/9/GRCh38#69733733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23684032-A-C

69734126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23683192-T-A

69734126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23683192-T-C

69734237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23683086-G-A

69734237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23683086-G-T

http://identifiers.org/hco/9/GRCh38#69734327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23683018-C-A

69734327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23683018-C-T

http://identifiers.org/hco/9/GRCh38#69741478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680832-C-A

69741514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23680796-T-C

http://identifiers.org/hco/9/GRCh38#69741522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680788-C-A

69741522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23680788-C-T

http://identifiers.org/hco/9/GRCh38#69741635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680682-A-C

69741739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23680559-T-A

69741739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23680559-T-C

http://identifiers.org/hco/9/GRCh38#69741813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680485-A-C

69741846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23680452-A-G

http://identifiers.org/hco/9/GRCh38#69741889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680413-A-C

69741889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23680413-A-G

69741903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23680399-T-C

http://identifiers.org/hco/9/GRCh38#69742014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680301-C-A

69742108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23680207-T-A

69742297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23680039-C-T

http://identifiers.org/hco/9/GRCh38#69742311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23680025-A-C

69742429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679977-T-C

69742770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679753-C-T

69742771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679752-A-G

69743056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679480-A-T

69743378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23678963-A-T

69743488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23678864-C-T

69743713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23678651-T-C

http://identifiers.org/hco/9/GRCh38#69745813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23676664-A-C

69745902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676571-G-A

69745963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676519-G-A

69745963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676519-G-C

69746341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676297-G-A

http://identifiers.org/hco/9/GRCh38#69746389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23676270-C-A

69746484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676188-T-C

69746627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676054-C-T

69746631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676050-T-C

69746663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676022-A-T

69746691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675994-C-T

69747205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23675573-T-C

http://identifiers.org/hco/9/GRCh38#69747215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23675558-A-C

69747550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675331-T-C

69747805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675086-T-C

69747899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23674976-C-T

69748635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23673757-A-G

69748657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23673736-T-C

69748760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23673653-T-C

69749090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23673409-T-C

69749383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23673121-T-C

69749616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672921-T-C

69749934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672640-A-G

69750044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672533-A-G

69750092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672500-A-G

69750155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672437-T-C

69750182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672423-A-T

69750204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672401-T-A

69750267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672329-G-A

69750278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672318-A-T

69750544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23672066-G-A

http://identifiers.org/hco/9/GRCh38#69750603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23672006-A-C

69750736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671893-T-C

69753587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23670374-T-C

http://identifiers.org/hco/9/GRCh38#69753736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23670255-A-C

69753736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23670255-A-G

69753778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23670209-A-T

http://identifiers.org/hco/9/GRCh38#69753842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23670150-C-A

69753862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23670130-C-G

69754011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23669970-T-C

69754045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23669321-T-C

69754208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23669168-A-G

69756104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668476-G-A

69756780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667977-T-C

http://identifiers.org/hco/9/GRCh38#69757016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23667711-C-A

69757016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667711-C-T

69757109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667463-C-G

69757197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23667293-T-C

69757848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666731-T-C

http://identifiers.org/hco/9/GRCh38#69758197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23666385-C-A

69758333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666268-A-G

69758377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666223-T-A

http://identifiers.org/hco/9/GRCh38#69758394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23666201-C-A

69758394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666201-C-G

69758394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666201-C-T

69758532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666066-T-C

69758575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666017-T-C

69758589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23666003-T-C

69758648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23665944-G-A

69758648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23665944-G-T

69758650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23665942-G-A

69758650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23665942-G-T

http://identifiers.org/hco/9/GRCh38#69758702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_lost
orthologous variants: http://identifiers.org/mco/19/GRCm39#23665895-C-A

69758702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 23665895-C-T

69758779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665823-A-G

69759644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23665079-G-A

http://identifiers.org/hco/9/GRCh38#69759685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23665039-C-A

69759789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23664967-A-G

69759992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23664772-G-A

69759992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23664772-G-T