74577459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154462613-G-A

http://identifiers.org/hco/1/GRCh38#74577853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462222-C-A

http://identifiers.org/hco/1/GRCh38#74577995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462079-A-C

74577995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154462079-A-G

74578161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461965-T-C

74578256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461870-A-G

74578376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461760-C-T

74578440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461699-C-G

http://identifiers.org/hco/1/GRCh38#74578455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154461684-C-A

74578465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461675-C-T

http://identifiers.org/hco/1/GRCh38#74578598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154461593-C-A

74578625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461566-T-G

http://identifiers.org/hco/1/GRCh38#74578635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154461556-C-A

74578635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154461556-C-T

74578791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461478-T-G

74579051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461223-C-T

74579181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461090-A-G

74579181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461090-A-T

74579370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

74579415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-G

74579456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-T

74582271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460208-A-T

74582352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460124-T-C

74582352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460124-T-G

74582396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460078-C-T

74582438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460047-A-T

74583872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459907-T-A

74583994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459786-A-G

74584057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459722-T-C

74584091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459690-C-T

74584262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459537-A-G

74584420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459348-G-A

74584527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459256-T-C

74584564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459122-T-C

74584637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459053-C-G

http://identifiers.org/hco/1/GRCh38#74584804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154458923-C-A

http://identifiers.org/hco/1/GRCh38#74584894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154458836-A-C

74584908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458831-T-C

74584961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458778-A-G

74586380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458551-C-T

74586570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458369-A-G

74586570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458369-A-T

74586577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458362-G-A

74586596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458347-T-C

74586596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458347-T-G

74586756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458161-G-A

74586757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458160-A-G

74586800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458121-G-T

74586831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458101-T-C

74586870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458065-T-C

74587384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457877-T-A

74587487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457783-A-G

74587522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457749-G-T

74587523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457748-A-G

74588149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154455713-C-G

74588374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154455508-A-G

74588560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154455355-C-T

74589179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454788-T-C

74589239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454734-A-G

74589246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454727-C-T

74589255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454718-T-C

74589423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454553-T-C

74589423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454553-T-G

74589545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454439-T-C

74589585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454407-T-C

74589743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454282-G-A

74589743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454282-G-C

74589811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454214-C-T

74589873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 154454158-T-G

74590159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453872-A-T

74590819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453587-A-G

74590909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453505-T-C

74590909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453505-T-G

74591059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453377-T-C

74591452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453021-G-A

74591799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154452672-T-C

74591939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154452532-T-A

http://identifiers.org/hco/1/GRCh38#74591989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154452469-C-A

http://identifiers.org/hco/1/GRCh38#74592108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154452353-C-A

74592108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154452353-C-T

http://identifiers.org/hco/1/GRCh38#74592204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154452285-C-A

74592573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451970-A-G

74592716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451832-T-A

74592968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451555-C-T

74593026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451504-A-G

74593038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451494-T-G

74593056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451484-G-C

74593130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451418-C-G

74593173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451376-A-G

74593174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451375-T-C

http://identifiers.org/hco/1/GRCh38#74594523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154451250-A-C

74594551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451222-C-T

74594984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450860-A-G

74594984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450860-A-T

74594993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450851-G-T

74595230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450622-A-T

74595272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450584-T-C

74596756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448870-G-T

74596823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448805-G-A

http://identifiers.org/hco/1/GRCh38#74596903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154448743-C-A

74596903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448743-C-T

74596904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448742-G-A

74596904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448742-G-T

74596988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448659-G-A

74597570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448116-T-C

74597632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448051-A-T

74599760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154444893-G-T

http://identifiers.org/hco/1/GRCh38#74599770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154444892-C-A

74599770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154444892-C-T

74600606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154444067-T-G

74600909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443769-G-A

74600909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443769-G-C

74600909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443769-G-T

74600911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443767-G-T

74600928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443750-A-G

74600986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443700-T-C

74601702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154441387-G-A

74602003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154441102-G-A

74602191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440949-A-T

http://identifiers.org/hco/1/GRCh38#74602252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154440874-A-C

74602314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440815-C-T

74602320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440809-T-C

74602344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440785-T-C

74602382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440747-C-T

74602386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440743-A-G

74602504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440644-G-A

74602761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440443-A-G

http://identifiers.org/hco/1/GRCh38#74602766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154440435-A-C

74603023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440213-G-A

74603026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440210-C-G

74603188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440070-G-A

74603395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439913-A-G

74605984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439777-G-A

74605984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439777-G-T

74606103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439696-A-G

74606125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439674-A-G

74606125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439674-A-T

74606210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439597-T-C

74606310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439499-T-C

http://identifiers.org/hco/1/GRCh38#74606390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154439421-C-A

74606390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439421-C-T

74606471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439357-T-G

74606496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439335-G-C

74606496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439335-G-T

74606513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439318-G-A

74606513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439318-G-T

74606739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154439123-A-T

http://identifiers.org/hco/1/GRCh38#74606804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154439058-C-A

74606813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154439049-T-C

74606954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438906-T-C

74606954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438906-T-G

74606976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438874-G-T

http://identifiers.org/hco/1/GRCh38#74606984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154438866-C-A

74606984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438866-C-T

74606985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438865-T-A

74606985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438865-T-C

74606985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438865-T-G

74607244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438514-T-C

74607506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438111-A-G

74607528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438093-G-A

74607597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438012-C-T

74608602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437554-C-T

74608743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437414-C-G

74608771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437388-C-T

74608792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437367-G-A

74608792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437367-G-C

74608875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437284-T-C

74609067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437100-G-A

74609894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436206-T-C

74609968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436133-T-C

74609978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436123-G-A

74609978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436123-G-T

74612345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433431-C-T

http://identifiers.org/hco/1/GRCh38#74612359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154433417-A-C

74612533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433291-A-T

http://identifiers.org/hco/1/GRCh38#74612584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154433250-C-A

74612584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433250-C-T

74612592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433246-G-A

74612592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433246-G-T

74612605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433231-G-A

74612605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433231-G-C

74612806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154433032-G-A

74612806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154433032-G-T

74613578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154432618-A-G

http://identifiers.org/hco/1/GRCh38#74613592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154432604-C-A

http://identifiers.org/hco/1/GRCh38#74613799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154432440-A-C

74613799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154432440-A-T

74614759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154431849-C-T

74614856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154431765-G-C

74614885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154431730-G-T

74615168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154431221-T-C

74615213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 154431177-T-C

74615244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 154431146-A-G

74615244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 154431146-A-T

http://identifiers.org/hco/1/GRCh38#74615268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154431122-A-C

74615368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154431017-G-T

74615882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154430352-A-G

74615948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154430288-G-A

74618432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154428136-A-T

74618439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154428129-C-G

74619041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154427551-C-T

74619052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154427540-A-G

74619072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154427521-T-C

http://identifiers.org/hco/1/GRCh38#74619120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154427474-A-C

74619120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154427474-A-T

74619826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426774-G-A

http://identifiers.org/hco/1/GRCh38#74620005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426622-C-A

74620005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426622-C-G

74620053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426581-G-T

http://identifiers.org/hco/1/GRCh38#74620514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426128-C-A

74620520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426122-A-G

http://identifiers.org/hco/1/GRCh38#74620620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426022-C-A

74620620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426022-C-G

74620620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426022-C-T

http://identifiers.org/hco/1/GRCh38#74620624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426018-A-C

74620624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426018-A-G

74620627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154426015-T-C

74620682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425960-A-T

74620684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425958-C-G

74620694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425948-A-G

74620726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 154425922-A-G

74620857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425791-A-G

74620981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425671-T-A

74620981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425671-T-C

74621007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425645-T-A

74621007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425645-T-C

http://identifiers.org/hco/1/GRCh38#74621044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154425610-C-A

http://identifiers.org/hco/1/GRCh38#74621264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154425444-C-A

74621371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425344-G-A

74621371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425344-G-T

74621382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 154425335-C-T

http://identifiers.org/hco/1/GRCh38#74621412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#154425305-C-A

74621442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 154425272-G-T

74621456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41093
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 154425260-T-G