http://identifiers.org/hco/14/GRCh38#75578677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#85793397-C-A

75578677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793397-C-G

75578677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793397-C-T

75578683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793403-G-A

75578683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793403-G-C

75578683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793403-G-T

75578686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793406-G-A

75578686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793406-G-T

75578688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793408-G-A

75578688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793408-G-T

75578706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85793411-G-A

75578706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85793411-G-T

75578817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793481-G-C

75578965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85793618-C-G

75579068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85793793-C-G

75579068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85793793-C-T

75579269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 85793991-C-G

75579506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 85794228-G-A

75579506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 85794228-G-T

75579701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794456-G-T

75579708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794463-G-T

75579738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794489-T-C

75579803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794582-C-T

75579878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794656-C-T

75580122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794869-A-G

75580151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794898-G-A

75580193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85794936-C-T

http://identifiers.org/hco/14/GRCh38#75580299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85795047-A-C

75580408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85795147-C-G

75580408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85795147-C-T

75587925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85800975-G-T

75588068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85801119-G-A

75595270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85801399-A-G

http://identifiers.org/hco/14/GRCh38#75595277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85801406-C-A

75595662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85801798-T-C

75595666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85801802-G-C

75595666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85801802-G-T

http://identifiers.org/hco/14/GRCh38#75595701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85801832-A-C

75595701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85801832-A-G

http://identifiers.org/hco/14/GRCh38#75598097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85803551-A-C

75598351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85803725-T-C

75598353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85803727-C-T

75599037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85804155-C-T

75599146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85804266-A-G

75599257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85804371-T-C

http://identifiers.org/hco/14/GRCh38#75604882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85810935-C-A

75604893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85810948-C-T

75604950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811020-G-A

75605148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811168-T-C

75605361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811354-T-A

http://identifiers.org/hco/14/GRCh38#75605373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85811366-C-A

75605373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811366-C-T

75605397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811389-T-C

75605441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811423-G-A

75605491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85811456-T-A

75605611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85811530-G-C

http://identifiers.org/hco/14/GRCh38#75605730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85811651-C-A

75605730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85811651-C-T

75607621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85815221-C-T

75607642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85815242-C-G

75607642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85815242-C-T

75607643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85815243-G-A

75609033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85816980-C-T

http://identifiers.org/hco/14/GRCh38#75609039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85816986-A-C

75609039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85816986-A-G

75609053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817001-C-T

75609174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817105-A-T

75609197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817127-A-G

75609315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817365-G-A

75609372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817423-T-G

75609462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817473-A-G

75609486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817498-G-A

75609561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817556-G-A

75609596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817593-T-C

75609610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85817617-C-G

75610175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85818222-G-C

75610290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85818327-C-T

75611288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85819646-G-A

75611300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85819658-G-T

75611398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85819750-G-A

75612048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85820190-C-T

75612218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85820268-T-C

75612368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85821235-T-C

http://identifiers.org/hco/14/GRCh38#75612407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85821272-C-A

75612430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85821299-G-A

75612552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85821411-C-G

75612552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85821411-C-T

75612635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85821496-C-T

75612799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85822293-C-T

75616436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85823647-T-A

75616851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85824143-G-C

75616863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85824155-T-G

75617189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85825103-G-A

75617688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85825792-G-C

75617691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85825795-C-G

75617882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85825965-T-G

75617999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85826052-A-T

75619798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85826562-G-C

75620578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85827338-T-C

75620600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85827360-T-A

75621019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85828202-A-G

75621458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85828849-G-T

75621540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85828917-C-T

75622186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85829838-T-C

75622272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85829915-A-G

http://identifiers.org/hco/14/GRCh38#75622343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85829985-C-A

75622343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85829985-C-G

75622515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85830171-C-T

75624414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85832664-A-G

75624670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85832920-G-A

75624670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85832920-G-T

75624709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85832959-G-A

75624709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85832959-G-C

75624764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833014-A-G

75624820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833052-T-C

75624862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833091-T-G

75624908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833114-T-C

75624952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833160-G-A

75625226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833693-A-G

75625315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85833795-C-T

75625497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85834143-G-A

http://identifiers.org/hco/14/GRCh38#75626025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85834579-C-A

75626747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85835845-C-T

75626892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85835951-T-C

75627114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85836173-G-A

75627143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85836421-C-T

75627164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85836442-G-A

75630102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85838478-C-T

75630797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839159-A-G

75631060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839400-T-C

75631169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839494-T-A

75631173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839498-C-T

75631204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839515-T-C

http://identifiers.org/hco/14/GRCh38#75631663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85839926-C-A

75631702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839970-G-C

75631702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85839970-G-T

75631786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85840073-G-A

75632047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85840688-T-C

75632050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85840691-A-G

75632241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85840870-T-C

75632308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85840931-T-C

http://identifiers.org/hco/14/GRCh38#75632489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85841118-C-A

75632489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85841118-C-T

75632578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85841211-G-T

75632736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85841479-T-A

75632736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85841479-T-C

75632833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85841658-G-A

75632886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85841715-G-A

http://identifiers.org/hco/14/GRCh38#75632895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85841724-C-A

75632990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85841848-T-G

http://identifiers.org/hco/14/GRCh38#75633345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85842654-A-C

75633395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85842702-A-G

75633468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85842777-A-G

75633594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85842917-G-T

75633751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85843060-G-T

75633839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85843147-G-T

75633888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85843196-T-C

75634446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85844630-T-C

75634599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85844867-G-A

75634604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85844872-G-A

75635049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85845408-A-G

75635049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85845408-A-T

http://identifiers.org/hco/14/GRCh38#75635122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85845495-C-A

75635122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85845495-C-G

75635122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85845495-C-T

http://identifiers.org/hco/14/GRCh38#75635150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#85845523-C-A

75635150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85845523-C-G

75635150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85845523-C-T

75635286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85845639-T-G

75635425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85845774-C-T

75635480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85845829-T-C

75635562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85845915-C-T

75636061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85846794-T-C

75636368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85847116-A-G

75636767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85847378-G-C

75636811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85847422-G-A

http://identifiers.org/hco/14/GRCh38#75636830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85847437-A-C

75636839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85847446-C-T

75636983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85847666-G-C

75637097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85847762-A-G

75637449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85848253-A-G

75637459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85848263-G-A

http://identifiers.org/hco/14/GRCh38#75637462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85848266-C-A

75637478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85848282-G-T

http://identifiers.org/hco/14/GRCh38#75637719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85848600-A-C

http://identifiers.org/hco/14/GRCh38#75637737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85848618-A-C

75637746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85848627-G-A

75638035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85848904-G-A

75638275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849091-G-A

75638306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849130-G-A

75638396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849203-C-T

75638415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849227-C-T

75639254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849805-A-G

http://identifiers.org/hco/14/GRCh38#75639260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85849811-C-A

75639260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849811-C-G

75639260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85849811-C-T

75639481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850038-T-C

75639482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850039-G-A

http://identifiers.org/hco/14/GRCh38#75639529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85850086-C-A

75639529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850086-C-G

75639529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850086-C-T

http://identifiers.org/hco/14/GRCh38#75639534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85850091-A-C

75639598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850156-G-A

75639598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850156-G-T

75640587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850816-G-A

http://identifiers.org/hco/14/GRCh38#75640636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85850863-C-A

75640636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850863-C-T

75640668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85850895-C-T

75640798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85851001-A-G

75641129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85851318-T-C

http://identifiers.org/hco/14/GRCh38#75641253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85851441-C-A

http://identifiers.org/hco/14/GRCh38#75641378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85851564-C-A

75641378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85851564-C-T

75641585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85851719-T-C

75641733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85851845-T-G

http://identifiers.org/hco/14/GRCh38#75641914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85852041-C-A

75641914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85852041-C-G

75641914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85852041-C-T

75641999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852119-G-A

75641999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852119-G-T

75642010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852130-G-C

75642049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852171-G-T

75642069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852349-T-A

75642101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852448-T-C

http://identifiers.org/hco/14/GRCh38#75642107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85852459-A-C

75642107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852459-A-G

75642130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85852482-C-T

75643387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85856411-T-C

75643410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85856431-T-G

75643451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85856470-C-T

75644079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85856938-T-G

75644759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85857551-G-A

http://identifiers.org/hco/14/GRCh38#75644971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85857718-A-C

75645716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85858358-G-A

75645968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85858509-G-T

75645998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85858538-G-A

75646044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85858585-G-A

75646323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85858738-A-G

http://identifiers.org/hco/14/GRCh38#75646503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85858921-A-C

75646571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85858988-G-T

75646584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85858996-G-A

75646629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85859046-T-A

http://identifiers.org/hco/14/GRCh38#75647009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85859374-C-A

75647009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859374-C-T

75647043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859408-A-G

75647051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859419-T-C

75647167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859531-G-C

75647167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859531-G-T

75647231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859570-T-G

75647249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859587-G-T

75647250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859588-G-A

75647250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859588-G-T

75647254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859592-T-C

75647277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859618-G-A

75647277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859618-G-T

http://identifiers.org/hco/14/GRCh38#75647484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85859774-A-C

75647484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859774-A-G

75647490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859780-G-A

75647490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859780-G-T

http://identifiers.org/hco/14/GRCh38#75647534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85859820-C-A

75647534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859820-C-G

75647534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859820-C-T

http://identifiers.org/hco/14/GRCh38#75647563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85859847-C-A

75647563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859847-C-T

http://identifiers.org/hco/14/GRCh38#75647592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85859875-C-A

75647592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859875-C-T

75647594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859877-A-T

http://identifiers.org/hco/14/GRCh38#75647630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85859913-C-A

75647630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85859913-C-T

http://identifiers.org/hco/14/GRCh38#75647769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85860055-C-A

75647769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860055-C-T

75647808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860076-G-T

75647823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860090-G-A

75647823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860090-G-T

75647871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860120-G-T

75647959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860154-T-C

http://identifiers.org/hco/14/GRCh38#75647961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85860156-C-A

75647961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860156-C-T

75647969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860159-C-T

75648061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860243-G-T

75648087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85860274-T-C

http://identifiers.org/hco/14/GRCh38#75648203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#85860392-C-A

75648203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85860392-C-T

75648768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85860858-T-C

75649539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85861229-A-G

75649587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85861277-C-G

75649587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85861277-C-T

75649670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85861373-T-C

http://identifiers.org/hco/14/GRCh38#75649806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85861486-C-A

75649806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85861486-C-T

75649884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85861546-C-T

75649992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85861650-C-T

75650304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85861732-G-T

75650349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85861753-G-T

75650670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862001-G-A

75650670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862001-G-T

75650850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862185-A-G

http://identifiers.org/hco/14/GRCh38#75650975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85862303-C-A

75651065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862389-T-C

75651144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862451-A-T

http://identifiers.org/hco/14/GRCh38#75651145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85862452-C-A

75651145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862452-C-T

http://identifiers.org/hco/14/GRCh38#75651421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85862702-A-C

http://identifiers.org/hco/14/GRCh38#75651455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85862790-C-A

75651500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85862836-G-A

75651735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863051-G-A

75651897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85863216-G-A

http://identifiers.org/hco/14/GRCh38#75652011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85863278-C-A

75652016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863283-G-T

75652091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863381-A-T

75652194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863503-G-A

75652194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863503-G-T

75652226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863542-T-C

75652297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863614-T-C

75652303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85863620-G-A

http://identifiers.org/hco/14/GRCh38#75652415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85863719-A-C

75653473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85864593-G-A

http://identifiers.org/hco/14/GRCh38#75653589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85864722-C-A

75653590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85864723-A-G

75653610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85864738-A-G

75653826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85864927-A-G

75653901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865019-T-C

75654252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865363-G-C

75654284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865397-T-A

75654284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865397-T-C

75654284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865397-T-G

75654384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865580-G-C

75654444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85865706-G-A

75654601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866011-G-T

75654670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866089-T-C

75654826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866195-G-A

75654826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866195-G-T

75654859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866226-G-A

75654859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866226-G-T

75655002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866370-G-A

75655002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866370-G-T

75655410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866616-G-A

75655410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866616-G-C

75655433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866628-G-A

75655733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85866914-T-C

75657040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868238-A-T

http://identifiers.org/hco/14/GRCh38#75657053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85868251-C-A

75657053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868251-C-T

75657258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868615-T-C

75657258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868615-T-G

75657264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868621-T-C

75657266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868623-G-T

75657290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85868646-T-C

75657452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85868944-G-A

75657482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85868974-C-T

75657513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85869005-A-G

75657553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869054-G-C

75657645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869392-T-C

75657656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869403-G-T

75657678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869425-T-A

75657685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869432-G-A

75657721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869472-T-C

75657806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869543-C-T

75657939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869664-A-G

75659082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85869860-C-T

75659584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870243-G-C

75659584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870243-G-T

75659713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870342-T-C

75659900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870481-C-T

http://identifiers.org/hco/14/GRCh38#75659901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85870482-A-C

75659903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870484-T-A

75659903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870484-T-G

75660071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870627-C-T

75660076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870632-G-A

http://identifiers.org/hco/14/GRCh38#75660217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85870772-A-C

75660412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85870928-C-T

75660722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85871211-A-G

75660722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85871211-A-T

75660777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85871247-G-A

http://identifiers.org/hco/14/GRCh38#75660835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871298-C-A

http://identifiers.org/hco/14/GRCh38#75660837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871301-C-A

75660837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85871301-C-G

75660837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85871301-C-T

http://identifiers.org/hco/14/GRCh38#75660848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871312-C-A

75660848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85871312-C-T

http://identifiers.org/hco/14/GRCh38#75660849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871313-A-C

75660849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85871313-A-G

75660886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85871350-T-C

http://identifiers.org/hco/14/GRCh38#75661017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871481-C-A

75661017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85871481-C-T

http://identifiers.org/hco/14/GRCh38#75661019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871483-C-A

75661333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85871806-A-G

http://identifiers.org/hco/14/GRCh38#75661358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871831-C-A

75661358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85871831-C-T

http://identifiers.org/hco/14/GRCh38#75661460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85871920-A-C

75661576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85872022-A-T

75661586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85872032-G-A

75661586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85872032-G-T

http://identifiers.org/hco/14/GRCh38#75661610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85872054-A-C

75662490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85872914-A-T

75662698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85873012-C-G

http://identifiers.org/hco/14/GRCh38#75662837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20105
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#85873052-A-C