173500495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064843-T-C

http://identifiers.org/hco/1/GRCh38#173500531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161064807-C-A

173500697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064680-T-G

173500838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064514-A-G

173500868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064484-T-C

173500913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064439-A-T

http://identifiers.org/hco/1/GRCh38#173500926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161064426-C-A

173500926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064426-C-T

http://identifiers.org/hco/1/GRCh38#173501010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161064361-C-A

173501010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064361-C-T

173501011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064360-G-A

173501011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161064360-G-T

173501131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064246-T-C

173501135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064242-A-G

173501140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064237-T-C

173501141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064236-T-A

173501141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064236-T-C

http://identifiers.org/hco/1/GRCh38#173501159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161064218-C-A

173501159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064218-C-T

173501161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064216-A-G

173501161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064216-A-T

173501176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064203-A-G

173501262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161064116-A-G

173503137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161063022-T-C

173503143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161063016-G-T

173503155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161063006-A-G

173503156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161063005-G-C

173503156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161063005-G-T

173503356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161062670-A-G

173503356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161062670-A-T

173503431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161062599-T-C

173503760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 161062339-G-A

173504829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061577-A-G

173504913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061486-G-A

173504916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061483-T-C

173505022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061405-G-A

http://identifiers.org/hco/1/GRCh38#173505124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161061298-A-C

173505124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061298-A-G

173505390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061060-C-T

173505408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061042-G-A

173505408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061042-G-T

173505421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061029-A-T

173505429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061021-G-T

173505433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161061019-A-G

http://identifiers.org/hco/1/GRCh38#173505443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161061009-C-A

173505462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161060960-T-G

173506808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161060253-T-C

173506810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161060252-G-T

173506944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 161060117-A-T

173507015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161060046-C-G

173507015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161060046-C-T

173507094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161059972-T-C

http://identifiers.org/hco/1/GRCh38#173507153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161059918-C-A

173507153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161059918-C-T

173507305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161059820-A-G

173507312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161059813-A-G

173507445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161059658-A-G

173508411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161058104-T-G

173508621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057925-C-G

173508879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057701-T-C

173508967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057654-G-A

173509160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057527-A-G

173509281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057401-T-A

173509481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057206-T-C

173509504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057183-G-A

173509504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161057183-G-T

173509712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161056981-G-T

173509812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161056885-A-G

http://identifiers.org/hco/1/GRCh38#173510082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161056420-A-C

173516199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161056204-C-T

http://identifiers.org/hco/1/GRCh38#173517458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161055667-C-A

173517458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161055667-C-T

173517514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161055615-T-G

173517803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161055327-A-G

173517821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161055306-C-T

173517822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161055305-A-G

http://identifiers.org/hco/1/GRCh38#173517843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161055284-C-A

173517843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161055284-C-T

173520554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052993-T-C

http://identifiers.org/hco/1/GRCh38#173520760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161052819-A-C

173520760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052819-A-G

http://identifiers.org/hco/1/GRCh38#173520845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161052750-C-A

173520859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052735-T-C

173520932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052668-C-G

173521158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052394-A-G

173521166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052386-T-C

http://identifiers.org/hco/1/GRCh38#173521272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161052279-A-C

173521272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161052279-A-G

173521344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161052208-T-C

173521353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161052199-T-C

http://identifiers.org/hco/1/GRCh38#173521356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161052196-C-A

173521356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161052196-C-T

173521386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161052166-A-T

http://identifiers.org/hco/1/GRCh38#173521425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161052129-A-C

173521425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052129-A-G

173521428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052126-A-G

173521428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052126-A-T

http://identifiers.org/hco/1/GRCh38#173521445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161052108-A-C

173521445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052108-A-G

173521614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161052000-T-C

173521719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051887-T-C

173521723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051883-T-C

173521726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051880-T-A

173521783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051830-A-T

173523935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051674-A-T

173524036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161051573-G-A

173524036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161051573-G-T

173524181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051429-T-A

http://identifiers.org/hco/1/GRCh38#173524266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161051389-C-A

173524367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051047-A-G

173524395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161051019-C-T

173524525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050912-G-A

173524662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050774-T-G

173524670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050753-G-C

173524670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050753-G-T

http://identifiers.org/hco/1/GRCh38#173524710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161050713-C-A

173524710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050713-C-G

173524710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050713-C-T

173524841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161050591-T-C

173524841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161050591-T-G

173524873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161050559-G-A

173524999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050443-T-C

173525070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050379-G-A

173525070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050379-G-T

http://identifiers.org/hco/1/GRCh38#173525172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161050293-A-C

173525232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050237-C-T

173525262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050209-G-A

173525288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050181-T-G

173525496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161050005-A-G

173525548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161049947-T-C

173526546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161048906-G-T

173527500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 161047679-C-T

173527727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161047451-C-G

http://identifiers.org/hco/1/GRCh38#173528136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161046923-C-A

173528202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161046858-G-A

173528399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161046660-T-C

173528600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161046292-T-A

173528739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161046169-T-C

173528788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161046120-T-C

173528841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161046068-T-C

173529074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161045854-G-C

173529791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161044586-C-T

173529882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161044480-A-G

173529960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161044402-T-C

173530085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161044279-T-C

173530134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161043779-G-A

173530134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161043779-G-T

http://identifiers.org/hco/1/GRCh38#173530156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161043757-C-A

173530346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161043582-G-A

173530378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161043551-C-G

http://identifiers.org/hco/1/GRCh38#173530447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161043487-C-A

173530452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161043482-C-T

173530727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161043301-G-A

173531249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161042781-G-A

http://identifiers.org/hco/1/GRCh38#173531763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

http://identifiers.org/hco/1/GRCh38#173533568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161040850-A-C

173533568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161040850-A-G

173533568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161040850-A-T

http://identifiers.org/hco/1/GRCh38#173533906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161040259-A-C

173533908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161040257-A-T

173533975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161040189-T-C

173534072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161040131-A-G

http://identifiers.org/hco/1/GRCh38#173534123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161040111-A-C

173534234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039975-A-G

http://identifiers.org/hco/1/GRCh38#173534373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161039874-C-A

173534381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039866-G-A

173534381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039866-G-T

173534395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039852-G-T

http://identifiers.org/hco/1/GRCh38#173534424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161039826-A-C

http://identifiers.org/hco/1/GRCh38#173534431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161039819-C-A

http://identifiers.org/hco/1/GRCh38#173534439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161039810-C-A

173534459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039790-A-G

173534491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161039758-G-A

173534694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039550-T-A

173534694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039550-T-C

173534696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039548-A-G

173534720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039525-A-G

173534725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039520-A-G

173534725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161039520-A-T

173535115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037966-G-A

173535349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037781-A-G

173535362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037768-T-G

173535747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037408-G-A

173535756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037403-A-T

173535830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 161037347-T-C

173535880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 161037297-A-G

173535929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161037248-A-T

173536041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037153-T-C

http://identifiers.org/hco/1/GRCh38#173536170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161037024-A-C

173536183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161037011-C-G

173536760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161036392-A-T

173536793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161036359-A-G

http://identifiers.org/hco/1/GRCh38#173536810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161036287-C-A

173536810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161036287-C-T

173536846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161036230-A-G

173536848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161036228-T-G

173536893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161036187-T-C

173547551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035430-T-A

173547551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035430-T-G

173547568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035413-T-C

173547586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035399-G-C

173547586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035399-G-T

173547598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035385-G-T

173547656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035329-G-A

173547817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035174-A-G

173547907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035086-A-T

173547957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035041-T-C

http://identifiers.org/hco/1/GRCh38#173547976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161035029-C-A

173548017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161035002-T-C

173548247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161034785-C-G

173548393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161033882-A-G

173548586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033681-A-G

173554116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033444-A-G

173554175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033387-T-C

173554520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033203-C-G

173554600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033125-T-A

173554647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033076-T-A

http://identifiers.org/hco/1/GRCh38#173554671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161033051-C-A

173554671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161033051-C-T

http://identifiers.org/hco/1/GRCh38#173554710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161033013-C-A

173554873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032851-A-G

173554948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032782-G-T

173554954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032779-T-A

173554954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032779-T-C

http://identifiers.org/hco/1/GRCh38#173555005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161032728-C-A

173555163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032627-T-C

173555164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032626-G-T

173555165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032625-G-A

173555165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032625-G-T

http://identifiers.org/hco/1/GRCh38#173555356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161032560-C-A

173555356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032560-C-T

173555367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032549-G-T

173555370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032546-G-A

173555395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032529-G-A

173555395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161032529-G-T

173555948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 161032086-C-T

173556117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161031933-A-G

173556118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161031932-G-T

173556119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161031931-C-T

173556345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161031636-A-G

173556999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161031185-T-G

173557002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161031182-G-T

173557017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161031167-T-C

173557117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161031104-G-A

173557231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161030986-T-A

173557560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161030655-T-C

173573281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161028424-G-A

173573281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161028424-G-C

173573332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 161028373-T-C

173573377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028329-A-T

http://identifiers.org/hco/1/GRCh38#173573420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161028285-C-A

173573420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028285-C-T

173573443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028262-T-A

173573443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028262-T-C

173573599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028118-T-C

173573721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028005-C-T

173573725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161028000-T-C

173573946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161027795-T-C

173574177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161027658-A-T

173574274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161027562-G-A

173574292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161027544-C-T

http://identifiers.org/hco/1/GRCh38#173574295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161027541-C-A

173574295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161027541-C-T

173574440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161027419-C-G

173576001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161026584-A-G

173576579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025953-T-A

173576579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025953-T-C

173576590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025942-T-C

http://identifiers.org/hco/1/GRCh38#173576644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161025887-C-A

173576644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025887-C-T

173576685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161025846-G-A

173576739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161025792-C-T

http://identifiers.org/hco/1/GRCh38#173576823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161025717-C-A

173576823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025717-C-G

173576823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025717-C-T

173576837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025703-A-G

173576837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025703-A-T

173576844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025696-G-T

173576863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025677-G-A

173576863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025677-G-C

173576863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025677-G-T

173577229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025355-G-T

173577247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025337-C-G

173577247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025337-C-T

http://identifiers.org/hco/1/GRCh38#173577387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161025247-A-C

173577433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161025211-T-C

173577671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161024987-T-C

173577681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161024974-A-G

173577687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161024968-G-A

173577883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161024781-C-T

173577887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161024777-T-C

173577915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161024702-T-C

http://identifiers.org/hco/1/GRCh38#173579885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161023988-C-A

173579888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161023985-A-G

http://identifiers.org/hco/1/GRCh38#173579938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161023930-C-A

173580652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161023646-C-T

173580689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161023614-T-A

173580926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161023378-A-G

173581308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161023065-T-C

173581550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022816-A-G

173581612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022755-A-G

173581730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022657-G-T

173581741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022647-G-C

173581741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022647-G-T

173581749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022626-A-G

173581749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022626-A-T

http://identifiers.org/hco/1/GRCh38#173581766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161022603-C-A

173581807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022567-A-G

http://identifiers.org/hco/1/GRCh38#173582032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161022338-A-C

173582032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022338-A-G

173582164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161022205-G-T

173582820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021707-A-G

http://identifiers.org/hco/1/GRCh38#173582861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161021673-C-A

173582894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021639-C-G

http://identifiers.org/hco/1/GRCh38#173583640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161021109-A-C

173583640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021109-A-G

173583658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021091-T-A

173583658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021091-T-C

173583658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021091-T-G

173583678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021071-G-A

173583678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021071-G-C

173583678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161021071-G-T

173587576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161010144-T-A

173587576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161010144-T-G

173587619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161010101-T-C

173587658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 161010067-G-A

173587972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161009776-T-A

173597334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161009145-T-C

http://identifiers.org/hco/1/GRCh38#173597443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161009041-A-C

173597709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161008801-A-G

173598067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161008526-C-T

http://identifiers.org/hco/1/GRCh38#173598565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161007570-C-A

173598808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161007339-C-T

173598839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161007309-T-C

173599014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161007142-G-T

173599089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161007071-T-G

173600246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006239-G-T

173600261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006231-A-G

173600274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006218-T-A

173600274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006218-T-C

173600274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006218-T-G

173600308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006193-A-T

173600482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161006016-T-C

173601055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161005557-T-C

173601520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161004738-A-T

173601538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161004720-T-C

173601577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161004688-T-C

173601670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161004605-C-G

173601763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161004512-A-G

http://identifiers.org/hco/1/GRCh38#173601847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161004460-C-A

173601849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161004458-T-C

173601849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161004458-T-G

173601874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161004398-G-T

http://identifiers.org/hco/1/GRCh38#173601885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#161004387-C-A

173601916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161004364-T-C

173602228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161003946-T-G

173602593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161003603-A-G

173602654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161003542-G-A

173602654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161003542-G-T

http://identifiers.org/hco/1/GRCh38#173602902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161003341-C-A

173602902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161003341-C-T

173602926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161003320-A-T

173603042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161003207-C-G

173603042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161003207-C-T

173603070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28664
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161003180-A-G