88059294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64672039-G-A

88059350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64671983-G-A

88059350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64671983-G-C

88059350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 64671983-G-T

88059434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64671899-G-A

88059434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64671899-G-C

http://identifiers.org/hco/3/GRCh38#88059545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64671788-C-A

88059545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671788-C-T

http://identifiers.org/hco/3/GRCh38#88059642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64671686-C-A

88059642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671686-C-T

http://identifiers.org/hco/3/GRCh38#88059655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64671669-C-A

88059655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671669-C-G

88059655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671669-C-T

88059666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671656-T-G

88059770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671544-G-A

http://identifiers.org/hco/3/GRCh38#88060010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#64671306-C-A

88060010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64671306-C-T

http://identifiers.org/hco/3/GRCh38#88060063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64671253-A-C

88060120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64671158-T-C

88060535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64670754-A-G

88061113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64670289-C-T

88061467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64669556-T-C

88061760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64669288-T-C

88061838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64669021-C-T

88062250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64668641-T-C

88062712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64668029-T-G

88062825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64667917-G-C

http://identifiers.org/hco/3/GRCh38#88062836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64667907-A-C

88062893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64667848-G-A

http://identifiers.org/hco/3/GRCh38#88063213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64667545-A-C

http://identifiers.org/hco/3/GRCh38#88063455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64667104-A-C

http://identifiers.org/hco/3/GRCh38#88063533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64667024-C-A

88063578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666980-A-G

88063663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666898-T-C

88063770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666786-T-C

88063791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666765-A-G

88064055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666265-T-C

88064102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666208-G-T

http://identifiers.org/hco/3/GRCh38#88064128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64666181-C-A

http://identifiers.org/hco/3/GRCh38#88064138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64666171-C-A

88064138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64666171-C-T

88064330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665999-T-G

http://identifiers.org/hco/3/GRCh38#88064372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64665971-C-A

88064518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665830-T-A

88064564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665782-T-A

88064632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665716-T-C

88064676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665673-C-T

88064916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665354-A-G

88065191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64665166-A-T

88065421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64664991-A-T

88067380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64663116-G-A

88067417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64663078-C-T

88067622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64662875-A-T

http://identifiers.org/hco/3/GRCh38#88067667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64662851-C-A

88067928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64662727-A-G

88067940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64662715-G-A

http://identifiers.org/hco/3/GRCh38#88068168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64662531-A-C

88073358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64659355-A-T

88073557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64659132-A-G

88073689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64659010-A-G

88073906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64658765-A-G

88075216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64657356-T-G

88075287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64657233-C-T

http://identifiers.org/hco/3/GRCh38#88075297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64657223-A-C

88075373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64657157-T-C

88075570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64656758-T-G

88076066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64656320-A-G

88076457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64655955-T-C

88076628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64655300-A-G

88076879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64655060-C-G

88077052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64654689-C-T

88077250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64654534-C-T

http://identifiers.org/hco/3/GRCh38#88077616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64654394-A-C

88078485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64652692-C-T

88078945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64652235-A-T

88079380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64651872-G-A

88079380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64651872-G-T

88079711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64651560-A-G

88079913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64651380-C-G

88079913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64651380-C-T

http://identifiers.org/hco/3/GRCh38#88086427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64650800-A-C

88086468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64650782-T-C

http://identifiers.org/hco/3/GRCh38#88087721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64650305-C-A

88088345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64649565-G-T

88088462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64649447-A-G

88088524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64649388-T-A

88088524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64649388-T-C

88091461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64646792-T-G

88092086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64644923-T-G

88092182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64644834-G-A

88092339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64644683-A-G

88092464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64644562-C-T

http://identifiers.org/hco/3/GRCh38#88092578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64644439-C-A

88093055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64644000-T-G

88093082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64643973-A-G

http://identifiers.org/hco/3/GRCh38#88112992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64635198-A-C

88113026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64635162-T-G

88113102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64635085-T-C

88113344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64634841-G-A

88113344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64634841-G-T

88113508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64634678-C-T

88114739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64624416-T-C

88114800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64624355-C-T

http://identifiers.org/hco/3/GRCh38#88114831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64624323-A-C

88115640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64623452-A-G

88117168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64622077-T-A

88117369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64621891-A-G

88117619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64621666-A-T

88119807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64618898-A-G

88119807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64618898-A-T

88122611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64617950-A-T

88124353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64616457-G-A

88124511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64616129-A-G

88124794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615843-C-T

88125562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615478-T-C

88125766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615305-A-G

88125770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615301-T-C

88125796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615275-T-C

88125949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615100-T-C

88126004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64615045-T-C

88126053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614997-G-T

88126116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614935-A-T

88126612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614554-A-T

88126706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614491-C-T

88126776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614401-T-C

88126826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614351-A-G

88127018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614144-T-C

88127087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64614069-G-A

88127260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64613971-C-T

88127794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64613248-T-C

88127913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64613130-T-G

88127975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64613083-C-T

88128748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64612384-G-A

88128748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64612384-G-T

88129137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64612022-A-G

88129137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64612022-A-T

88129144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64612015-G-C

88129164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611997-C-G

88129164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611997-C-T

88129356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611889-A-G

88129361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611884-G-A

88129361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611884-G-T

http://identifiers.org/hco/3/GRCh38#88129543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64611722-A-C

http://identifiers.org/hco/3/GRCh38#88129556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64611709-C-A

88129556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611709-C-G

88129556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611709-C-T

http://identifiers.org/hco/3/GRCh38#88129582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64611690-A-C

88129582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611690-A-T

http://identifiers.org/hco/3/GRCh38#88129768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64611506-C-A

88129856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611419-T-C

88129883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611392-T-C

88129883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611392-T-G

88129890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64611378-T-A

88134729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64609109-A-G

88134772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64609064-T-C

88135043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64608824-T-C

88135324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64608624-A-G

88135536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64608442-T-A

88135536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64608442-T-C

88135536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64608442-T-G

88137938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64608343-C-T

88138153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64608164-C-T

88138165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64608152-G-A

88138647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron variant
orthologous variants: 64607215-T-C

http://identifiers.org/hco/3/GRCh38#88139135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64606733-C-A

88139135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606733-C-T

88139191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606695-G-A

88139191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, stop_gained
orthologous variants: 64606695-G-T

88139212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606674-G-A

http://identifiers.org/hco/3/GRCh38#88139261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64606625-C-A

88139261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606625-C-G

88139261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606625-C-T

http://identifiers.org/hco/3/GRCh38#88139299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64606587-A-C

88139549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606337-C-T

88139707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606179-G-A

http://identifiers.org/hco/3/GRCh38#88139710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64606176-A-C

88139710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606176-A-G

88139836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606056-G-A

88139842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606050-C-G

88139842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64606050-C-T

88139902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64605990-A-G

88140299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64605593-C-G

88140415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64605501-A-G

88140663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64605253-T-A

88140663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64605253-T-C

88140676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: intron_variant, missense_variant
orthologous variants: 64605240-A-G

http://identifiers.org/hco/3/GRCh38#88141152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64604761-C-A

http://identifiers.org/hco/3/GRCh38#88141203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64604716-C-A

88141210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64604709-A-G

88141622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64603657-A-G

88141622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64603657-A-T

88141764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64603519-T-C

88141933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 64603347-A-G

88141933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 64603347-A-T

http://identifiers.org/hco/3/GRCh38#88141999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#64603274-C-A

88141999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 64603274-C-T

http://identifiers.org/hco/3/GRCh38#88142049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64603234-A-C

88142049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64603234-A-G

88142049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64603234-A-T

88142214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64603062-A-G

88142375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64602911-C-T

http://identifiers.org/hco/3/GRCh38#88142535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64602747-C-A

88142638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64602646-A-G

88143081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64602222-A-G

88143140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64602167-A-G

88143459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601858-T-G

88143512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601805-T-C

88143680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601630-T-C

88143680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601630-T-G

88143790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601512-G-T

88144011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601304-G-A

88144011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601304-G-T

88144231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601130-T-G

88144293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64601069-T-C

http://identifiers.org/hco/3/GRCh38#88144420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#64600948-C-A

88144501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64600870-G-A

88144660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25612
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64600708-A-G