http://identifiers.org/hco/4/GRCh38#174637213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56582807-C-A

http://identifiers.org/hco/4/GRCh38#174637378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56582684-A-C

http://identifiers.org/hco/4/GRCh38#174637538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56582519-C-A

174637564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56582489-G-A

174637579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56582476-A-G

174637655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56582400-C-T

174637691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56582364-A-G

http://identifiers.org/hco/4/GRCh38#174637793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56582273-A-C

174637862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56582204-T-G

174640429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56581531-T-C

174640625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56581357-T-C

174640656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56581327-T-C

http://identifiers.org/hco/4/GRCh38#174640851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56581136-C-A

174641429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580550-G-T

174641439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580536-C-T

174641461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580514-T-C

174641462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580513-T-C

174641469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580506-G-A

174641469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580506-G-T

174641509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56580466-A-G

174642222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579758-T-C

174642282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579697-T-C

174642372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579607-G-T

174642635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579410-T-A

174642738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579308-T-A

174642760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579289-T-C

174642995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56579059-A-G

174643270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578852-G-A

174643270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578852-G-T

174643304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578822-A-G

174643304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578822-A-T

174643346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578780-T-G

174643433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578670-G-A

174643433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578670-G-C

174643433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578670-G-T

174643726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 3 prime UTR variant
orthologous variants: 56578441-A-G

174643890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense variant
orthologous variants: 56578281-T-C

174644136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56578040-T-A

174644373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56577839-A-T

174644432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56577780-T-A

174644432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56577780-T-C

174644462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56577750-T-C

174644477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56577735-C-T

174644543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56577669-C-G

174645445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576820-G-A

174645445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576820-G-C

174645445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576820-G-T

174645456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576809-T-C

174645541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576726-G-A

http://identifiers.org/hco/4/GRCh38#174645619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56576650-C-A

http://identifiers.org/hco/4/GRCh38#174645852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56576397-A-C

174645854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576395-T-A

174646175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576194-A-T

174646340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56576041-T-C

http://identifiers.org/hco/4/GRCh38#174646377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56576012-A-C

http://identifiers.org/hco/4/GRCh38#174646931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56575560-C-A

174647755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56574362-C-T

174647857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56574275-A-G

174648001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56574130-T-G

174648061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56574082-G-C

174648130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56574026-G-A

174648518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573941-C-G

174648918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573597-G-A

174648918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573597-G-C

174648926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573589-G-C

174648946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573569-C-T

174649009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573514-A-T

174649100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573390-A-G

174649209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573294-C-G

174649349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56573149-G-A

174649584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572913-G-A

174649675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572519-G-T

174649775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572448-G-A

174649844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572379-A-G

174649844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572379-A-T

174649862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572369-T-A

174650102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572136-G-A

174650102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572136-G-T

174650216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572030-A-G

174650222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56572024-T-C

174650427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56571854-T-C

http://identifiers.org/hco/4/GRCh38#174650780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56571458-C-A

174652220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56571089-A-T

174652416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570860-C-T

http://identifiers.org/hco/4/GRCh38#174652463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56570808-C-A

174652463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570808-C-T

174652738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570297-A-G

174652782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570259-T-C

174652785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570256-T-C

174652911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570128-T-A

174652911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56570128-T-C

http://identifiers.org/hco/4/GRCh38#174652982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56570038-C-A

174653079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569955-G-A

174653118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569917-A-G

174653227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569814-T-G

174653251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569793-G-C

174653377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569683-C-T

174653395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569670-A-G

174653419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569645-C-T

174653812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569243-C-T

174653816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56569239-T-C

174653896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568884-A-G

174653901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568880-C-T

174653911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568870-A-G

174653925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568862-A-T

174654174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568630-T-C

174654593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568242-C-G

174654593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568242-C-T

174654704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56568132-C-G

174655025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56567833-A-G

174655235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56567626-A-G

174655963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566756-G-T

174656002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566715-G-A

174656039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566677-G-C

174656316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566451-T-C

174656346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566422-T-C

174656453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566171-A-T

174656602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron variant
orthologous variants: 56566044-A-G

174656820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565830-G-A

174656820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565830-G-T

174656833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565817-A-G

http://identifiers.org/hco/4/GRCh38#174656886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56565774-C-A

174656950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565711-T-C

174657275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565396-T-C

174657349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565337-C-T

174657390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565296-G-A

174657569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565145-A-G

174657571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565143-C-T

174657609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565065-G-A

174657650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565024-G-A

174657721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56564915-A-G

http://identifiers.org/hco/4/GRCh38#174657745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56564885-A-C

174657745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56564885-A-G

174657768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56564815-T-A

174657849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56564738-G-T

174658132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56564514-G-C

http://identifiers.org/hco/4/GRCh38#174658313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56564341-C-A

174658379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56564275-C-T

http://identifiers.org/hco/4/GRCh38#174658576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56564076-A-C

174658756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563910-A-G

174658792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563875-T-C

174658920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563760-A-G

174658920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563760-A-T

174658987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563690-A-G

174658987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563690-A-T

174659006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563672-T-C

174659006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563672-T-G

174659106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56563571-A-G

174659172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56563505-A-G

174659240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563437-T-C

174659369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563291-T-C

174666059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553202-A-G

174666213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553093-T-C

174666297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553034-T-C

174666309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553022-T-A

174666309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553022-T-C

174666320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553011-T-A

174666320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553011-T-C

174666332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552999-G-A

174666377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552951-G-A

http://identifiers.org/hco/4/GRCh38#174668304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56550617-A-C

174668304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550617-A-G

174668513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550414-C-T

174668610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550317-C-T

174668635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550292-G-T

174668937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549882-G-T

http://identifiers.org/hco/4/GRCh38#174669181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56549686-C-A

http://identifiers.org/hco/4/GRCh38#174669471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56549430-A-C

174669503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56549398-A-T

174669909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549301-T-C

174669989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549224-C-T

174670237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548982-T-C

174670360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548860-T-C

174670549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548632-T-C

174670554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548626-T-A

174670764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548317-G-C

174670912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548192-T-A

http://identifiers.org/hco/4/GRCh38#174671027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56548072-A-C

174672075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546612-A-G

174672106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546582-G-T

174672313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546351-A-G

174672659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546023-A-G

174672691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546000-T-C

174672740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545949-G-A

174672740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545949-G-C

174673310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545756-C-T

174673324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545732-T-G

http://identifiers.org/hco/4/GRCh38#174673390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56545684-C-A

174673390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545684-C-T

174673415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545657-A-T

174673592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545485-G-A

174673632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545461-T-C

174673661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545432-C-T

174673924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545196-C-G

174674032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545118-C-T

174674155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545051-C-T

174674346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544868-A-G

174674613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544505-A-T

174674794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544318-G-T

174674807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544308-G-C

174674859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544258-T-C

174675005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544077-G-A

174675228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543856-G-T

174675267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543819-T-G

174675366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543715-T-C

174675678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543396-T-A

174675678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543396-T-C

174675696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543378-T-C

174675915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543138-G-A

http://identifiers.org/hco/4/GRCh38#174675942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56543113-C-A

174676025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543037-A-G

174676076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542995-G-A

174676110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542964-A-G

174676122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542952-T-G

174676227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542849-T-C

174676397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542693-A-G

174676404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542686-G-T

174676448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542639-T-C

http://identifiers.org/hco/4/GRCh38#174676635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56542551-C-A

174676776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542495-A-G

174676854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542420-G-A

http://identifiers.org/hco/4/GRCh38#174677007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56542285-C-A

174677007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542285-C-G

174677054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542255-T-C

174677181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56542128-A-G

174677181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56542128-A-T

http://identifiers.org/hco/4/GRCh38#174677414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56541946-A-C

174677414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541946-A-G

174677414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541946-A-T

174677546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541918-G-A

174677546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541918-G-T

http://identifiers.org/hco/4/GRCh38#174677617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56541905-C-A

174677656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541879-G-A

174677722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541859-G-A

174677961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541658-G-A

174677961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541658-G-T

174677965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541653-T-C

http://identifiers.org/hco/4/GRCh38#174678120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56541514-A-C

174678374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541300-T-G

174678943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540755-T-A

174680871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540093-C-T

174681024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539935-G-T

174681039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539920-T-C

174681062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539888-C-T

174681099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539863-A-G

174681099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539863-A-T

174681122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539838-C-T

174681123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539837-G-A

174681123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539837-G-C

174681526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539499-C-G

174681526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539499-C-T

174681586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539435-T-C

174681588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539433-G-C

174681642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539377-C-T

174681643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539376-G-A

174682242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538833-G-A

174682275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538800-G-A

174682415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538662-T-A

174682551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538515-T-C

174682621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538447-C-G

174682670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538401-G-A

174682670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538401-G-T

http://identifiers.org/hco/4/GRCh38#174682728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56538357-C-A

174682834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56538252-T-C

174683100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537992-T-A

174683175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537950-C-T

http://identifiers.org/hco/4/GRCh38#174683176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56537949-C-A

174684490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537544-T-C

174685341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537163-C-G

174685402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537102-G-A

174685861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536499-G-A

174685908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536452-T-C

174686442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535919-T-C

174686491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535878-T-C

174686545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535838-T-C

174686935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535622-T-A

174687245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535349-T-C

174696288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

174696321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

174696390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

174697147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530396-A-G

174697185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530358-C-T

174697364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530155-A-T

174697645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529887-T-G

174697706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529830-A-G

174697803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529757-C-T

http://identifiers.org/hco/4/GRCh38#174697821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56529739-A-C

174697821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529739-A-G

174697872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529688-C-T

174697902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529648-G-A

http://identifiers.org/hco/4/GRCh38#174698055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56529503-C-A

http://identifiers.org/hco/4/GRCh38#174698722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56529189-A-C

174698778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529132-A-G

174698855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529044-G-A

174698860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529039-T-A

174698868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529031-A-G

174698869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529030-G-C

http://identifiers.org/hco/4/GRCh38#174698908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56529018-C-A

174699326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528924-T-C

174699659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528622-A-G

174699677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528606-A-T

174699924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528486-A-G

174699927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528483-T-C

174700095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528321-G-A

174700152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528273-C-T

174703709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527138-G-A

174703721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527126-T-G

174703876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526976-A-G

174705499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525607-G-C

174705614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525496-A-G

http://identifiers.org/hco/4/GRCh38#174705713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56525392-C-A

174705713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525392-C-G

174705713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525392-C-T

174705757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525354-T-C

174705757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525354-T-G

174708098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56523224-C-G

http://identifiers.org/hco/4/GRCh38#174708224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56523103-A-C

174708224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56523103-A-G

http://identifiers.org/hco/4/GRCh38#174708383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56522947-A-C

174713410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518311-G-A

174713460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518260-T-C

http://identifiers.org/hco/4/GRCh38#174713666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56518066-C-A

174713788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517954-T-A

174713788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517954-T-C

174713845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517896-T-G

http://identifiers.org/hco/4/GRCh38#174713896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56517851-A-C

174713905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517842-G-T

174713997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517746-C-T

174713998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517745-T-G

174714322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56516588-T-C

174714334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56516567-A-T

http://identifiers.org/hco/4/GRCh38#174714387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56516508-A-C

174714458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56516436-A-G

174714537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56516360-A-T

174714602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56516292-G-A

174714651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56516242-G-A

174714651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56516242-G-C

174715060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515818-G-A

174715167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515713-G-A

174715203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515675-T-C

174715410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515622-A-G

http://identifiers.org/hco/4/GRCh38#174715571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56515463-C-A

174715571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 56515463-C-T

174715599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515434-G-T

174715688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515345-T-C

174715870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56509113-C-T

174715882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56509101-A-G

http://identifiers.org/hco/4/GRCh38#174716050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56508928-C-A

174716055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508923-G-C

174716074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508904-G-C

174716274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508677-T-C

174716412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508542-C-T

174716610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508318-T-A

174716624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508305-T-C

174716874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508078-T-C

174717472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507941-C-T

http://identifiers.org/hco/4/GRCh38#174717652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56507750-C-A

174717781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507610-A-T

174717952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507439-A-G

http://identifiers.org/hco/4/GRCh38#174718032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56507360-C-A

174721817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500082-G-A

174721822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500077-T-C

174721885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500014-A-G

174721888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500011-T-C

174722391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499578-A-T

174722395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499574-C-T

174722463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499509-C-G

174722463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499509-C-T

174722618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499363-G-A

http://identifiers.org/hco/4/GRCh38#174722638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56499343-C-A

174722638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56499343-C-T

174723067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498926-G-T

174723302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498722-A-G

174723318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498706-G-A

174723364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498660-T-C

http://identifiers.org/hco/4/GRCh38#174725884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56494820-A-C

174726027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494649-T-C

174726032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494644-G-T

174726134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494572-G-T

174726262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494460-G-C

174726262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494460-G-T

174726428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494316-T-A

174726744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494032-A-G

174726783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493996-G-C

174726783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493996-G-T

174727204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493661-G-A

174727210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493655-G-A

174727289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493578-C-G

http://identifiers.org/hco/4/GRCh38#174727541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56493325-C-A

174727541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493325-C-G

174727589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493287-T-C

174728174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493122-T-C

http://identifiers.org/hco/4/GRCh38#174728408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56492906-A-C

174728408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492906-A-G

174728435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492877-T-C

174728435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492877-T-G

174728453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492859-G-A

174728453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492859-G-T

174728460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492852-A-T

174728655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56492658-G-A

174728847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492535-T-C

174728965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492465-A-G

174728977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492446-G-C

174728989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492435-A-G

174729174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492271-T-C

174729185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492260-G-T

174729277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492171-A-G

174729344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492095-C-T

174729428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491847-G-A

174729583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491579-T-A

174729604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491526-T-C

http://identifiers.org/hco/4/GRCh38#174729779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56491371-A-C

174729968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491219-T-A

174730015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491174-T-C

174734172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56490202-T-A

174734372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56490024-A-G

174734498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489900-A-G

174735004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489432-G-A

174735034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489403-A-G

174735125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489331-T-C

http://identifiers.org/hco/4/GRCh38#174735127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56489329-C-A

174735270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489196-C-G

174735274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489192-A-G

174735274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489192-A-T

http://identifiers.org/hco/4/GRCh38#174735276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56489190-C-A

174735276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489190-C-T

174735317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489172-T-G

174735338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489151-T-G

174735424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489064-T-G

174735556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488932-G-A

http://identifiers.org/hco/4/GRCh38#174736132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56488797-A-C

174736159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488774-A-G

http://identifiers.org/hco/4/GRCh38#174737149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56486972-A-C

174737149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486972-A-G

174737388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486391-T-C

174738064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486058-T-C

174738477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485585-G-A

174738641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485429-A-T

174738725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485335-G-T

174738959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484497-T-C

174738977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484478-C-T

174741954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484222-A-G

174741978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484208-G-T

http://identifiers.org/hco/4/GRCh38#174751253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56476267-C-A

174751253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56476267-C-T

174751478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56476033-C-G

174751478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56476033-C-T

174751536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475970-A-G

174751673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475856-T-C

174751698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475831-G-A

http://identifiers.org/hco/4/GRCh38#174751930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56475506-A-C

174752064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475369-C-T

http://identifiers.org/hco/4/GRCh38#174752078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56475354-A-C

174752234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475209-G-A

174752300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475150-A-G

174752564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474857-G-A

http://identifiers.org/hco/4/GRCh38#174752570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56474851-A-C

174752570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474851-A-G

174752861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474573-A-G

174752861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474573-A-T

174752918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474516-G-T

174753333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474058-C-T

174753475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473947-C-T

http://identifiers.org/hco/4/GRCh38#174753543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56473879-C-A

174754055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473394-A-G

174754178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473277-G-A

174754288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473166-T-A

174754428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473042-A-G

174754682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472831-T-A

174754956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472076-G-A

174755279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471760-G-A

174755294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471746-T-G

174755430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471618-A-T

174755638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471521-T-A

174755640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471519-C-T

174756030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470976-T-C

174756362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470754-A-G

174760915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462651-T-A

174760915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462651-T-C

174760924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462642-A-G

174761112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462453-G-A

174761245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462335-G-T

174761344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462263-C-T

174761360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462247-A-G

174761650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461965-G-A

174764331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461541-C-T

174764335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461537-A-G

174764352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461520-T-A

174764352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461520-T-C

174764444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461427-T-C

174764484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461387-T-C

174764531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461306-T-A

http://identifiers.org/hco/4/GRCh38#174764536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56461301-C-A

174764573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461211-G-A

174764697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461012-G-C

174764786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460923-T-G

174764824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460885-C-T

174765028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460687-A-G

174765161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460566-G-A

174765230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460528-T-C

174765274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460487-T-C

174765437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460370-C-T

http://identifiers.org/hco/4/GRCh38#174765469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56460337-A-C

174765615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460190-T-A

174765615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460190-T-C

174765663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460142-T-G

http://identifiers.org/hco/4/GRCh38#174765676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56460131-C-A

174765676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460131-C-T

174766629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458523-T-A

174766698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458459-A-T

174766822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458332-G-T

174766876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458280-T-G

http://identifiers.org/hco/4/GRCh38#174766985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56458195-C-A

174766985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56458195-C-T

174767027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56458153-G-A

174767027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56458153-G-T

http://identifiers.org/hco/4/GRCh38#174767079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56458099-C-A

174767079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458099-C-T

http://identifiers.org/hco/4/GRCh38#174767104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56458074-C-A

174767104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458074-C-T

http://identifiers.org/hco/4/GRCh38#174767148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56458024-A-C

174767148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56458024-A-G

http://identifiers.org/hco/4/GRCh38#174767164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56458008-A-C

http://identifiers.org/hco/4/GRCh38#174767165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56458007-A-C

174767287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457804-A-G

174767435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457668-G-T

174767476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457600-T-C

174767485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457591-A-G

174767585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457507-A-T

174767611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457483-G-A

174767648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457448-C-T

174767672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457425-C-T

174767682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457416-G-A

174767682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457416-G-T

174767730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457390-A-G

174767810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457320-T-A

174767906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457244-C-T

174768027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457141-T-C

174768336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456866-A-T

174768344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456859-T-C

174768447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456774-C-G

174768447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456774-C-T

174768462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456759-A-G

http://identifiers.org/hco/4/GRCh38#174768535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56456684-C-A

174772122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452513-G-A

174772373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452180-G-A

174772373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452180-G-T

174772635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451985-C-T

174772745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451883-G-T

174772747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451881-A-G

174772903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451339-T-A

174772903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451339-T-C

http://identifiers.org/hco/4/GRCh38#174773293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56450951-C-A

174773341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450909-G-A

174773341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450909-G-T

174773557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450702-G-C

174773758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450538-C-T

174773805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450518-C-T

174773983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450338-G-A

174774109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450214-G-A

174774121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450202-C-T

174775393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450079-A-G

174775393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450079-A-T

174775508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449968-T-C

174775512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449964-A-G

http://identifiers.org/hco/4/GRCh38#174775728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56449772-A-C

174775751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449752-T-A

174775920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449411-A-G

174775929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449401-G-A

174786768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56447741-T-A

174786768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56447741-T-C

174786810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56447695-G-T

http://identifiers.org/hco/4/GRCh38#174786813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56447692-C-A

174787009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56447503-C-G

174787302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56446486-T-C

174787376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56446429-C-G

174787689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56446341-A-G

174787711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56446318-A-G

174787756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56446273-A-G

http://identifiers.org/hco/4/GRCh38#174788635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56444459-C-A

174788650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444444-G-A

174788650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444444-G-T

174788679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444414-G-A

174788679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444414-G-C

174788679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444414-G-T

174788783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444314-A-G

174788893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56444209-A-G

174788893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56444209-A-T

174788937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56444165-A-G

174788937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56444165-A-T

http://identifiers.org/hco/4/GRCh38#174788981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56444121-A-C

174788981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444121-A-G

174789000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444107-T-C

174789042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444069-G-A

174789042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444069-G-T

http://identifiers.org/hco/4/GRCh38#174789058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56444051-C-A

http://identifiers.org/hco/4/GRCh38#174789065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56444044-A-C

174789065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444044-A-G

174789066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444043-T-A

174789087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444025-A-G

174789121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443991-T-C

174789167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443949-C-T

174789273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443846-C-G

174789418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443702-T-A

174789458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443665-A-T

174789582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443562-T-C

174789655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443520-C-T

174789676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443498-C-T

174789775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443422-C-G

174794030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436899-T-A

174794150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436774-A-T

174794189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436737-C-T

174794272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436662-G-A

174794287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436647-A-G

174794522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56435063-T-C

174794538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56435046-T-A

http://identifiers.org/hco/4/GRCh38#174794752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56434775-C-A

174795140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427966-T-A

174795140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427966-T-C

174795274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427829-A-G

174795311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427792-T-C

174795320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427783-T-C

174795412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427713-T-G

174795506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427616-G-A

174795649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427486-C-T

174795786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422661-T-G

174795797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422649-A-T

174795806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422640-G-T

http://identifiers.org/hco/4/GRCh38#174795844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56422603-A-C

174795877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422573-C-T

174795934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422511-T-A

174795943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422502-A-G

174796019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422439-T-C

174796091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422384-T-C

174796103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422373-G-T

174796104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422372-G-C

174796182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422305-T-C

http://identifiers.org/hco/4/GRCh38#174796192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56422295-C-A

174796192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422295-C-T

174796227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422263-A-G

174796258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422231-A-G

174796297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56422192-A-G

174796904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421928-A-G

174796904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421928-A-T

174796982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421862-T-A

174796990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421854-C-T

174797103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421757-C-G

http://identifiers.org/hco/4/GRCh38#174797106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56421754-A-C

174797192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421663-G-A

174797192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421663-G-T

http://identifiers.org/hco/4/GRCh38#174797194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56421661-A-C

174797267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421598-G-A

174797413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421465-T-A

174797459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421425-G-A

174797460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421424-T-A

http://identifiers.org/hco/4/GRCh38#174797545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56421340-A-C

174797549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56421336-T-A

http://identifiers.org/hco/4/GRCh38#174798379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56420512-C-A

174798379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420512-C-T

174798413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420480-T-C

174798452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420440-G-A

174798497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420395-G-A

174798500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420392-T-C

174798500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420392-T-G

174798573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420325-A-G

174798622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420286-G-T

174798982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420233-C-T

174799013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420203-C-T

174799069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420149-T-C

174799189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420054-T-C

174799229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419981-G-A

174799229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419981-G-C

174799277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419926-T-C

174799477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419641-C-G

174799492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419626-C-T

174799819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419296-A-G

174799912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419067-G-T

174800016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418839-A-T

174803278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418151-G-A

174803524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417900-T-C

174804074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417335-T-C

174809829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412632-T-A

174810088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412377-A-G

174810404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410557-G-C

174810447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410512-A-G

174810678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410280-G-A

174810678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410280-G-T

http://identifiers.org/hco/4/GRCh38#174810980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56410000-C-A

174810980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410000-C-G

174811182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409793-C-T

174811188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409788-T-C

174811189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409787-T-G

174811218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409761-A-G

174811366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409720-G-T

http://identifiers.org/hco/4/GRCh38#174811531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56409561-C-A

174811767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409338-A-G

174812216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56408829-C-T

174812258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56408785-G-A

174812660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56408391-A-G

174812792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407795-G-C

174812972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407649-C-T

http://identifiers.org/hco/4/GRCh38#174812978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56407643-C-A

174813120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407482-A-G

174818169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405737-G-A

174818388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405566-C-T

174818414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405540-C-T

174818528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405428-A-G

174818615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405339-G-A

174818631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405317-G-C

174818631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405317-G-T

174818762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405187-A-G

174818762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405187-A-T

174818890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405057-G-T

174818928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405023-G-T

174818986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404967-T-G

http://identifiers.org/hco/4/GRCh38#174818987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56404966-C-A

174818987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404966-C-T

174819193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404409-T-C

174819379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404181-G-T

174819389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404171-G-A

174819460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404109-A-T

174819556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404002-A-T

174819611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403943-A-T

174819808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403748-G-A

174819888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403675-T-C

174819895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403664-T-G

174819971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403582-C-T

174820488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403127-C-G

174820525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403095-A-G

174820573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403048-T-G

174820594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403026-G-T

174820694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402929-G-A

174820694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402929-G-C

174820798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402838-C-T

174820844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402792-C-T

174821038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402635-A-G

174821057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402623-T-G

174821229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402458-T-C

174821271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402417-T-C

174821476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402157-T-A

174821534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402102-T-C

174821725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401894-C-T

http://identifiers.org/hco/4/GRCh38#174822047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56401628-C-A

174822138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401559-A-G

174822216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401477-T-C

174822218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401475-C-T

174822282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401411-C-G

174822290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401403-C-T

174822292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401401-T-C

174822292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401401-T-G

174822366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401339-A-G

174822373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401332-C-T

174822439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401241-T-C

174822522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400511-A-G

174822588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400442-T-C

174822826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400219-T-C

174822990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400069-G-T

174823081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399989-T-C

174823160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399927-T-C

174823173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399920-C-T

http://identifiers.org/hco/4/GRCh38#174823229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56399864-A-C

174823236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399856-T-A

174824545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398302-A-G

174824584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398263-A-T

174824726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398131-C-G

174824726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398131-C-T

174825579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397293-T-C

174825818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396999-T-C

174825915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396852-A-G

174825972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396802-A-G

174826105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396610-T-G

174826283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396399-T-A

174826393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396285-T-C

174826505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396173-G-C

174826892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395788-A-G

174826892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395788-A-T

174826899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395782-A-G

174826899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395782-A-T

174826910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395771-G-A

174826910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395771-G-C

174826910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395771-G-T

174826923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395758-A-T

174827008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395707-G-T

174827134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395595-T-G

174827293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395461-A-G

174827421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395352-A-G

174827627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395122-A-T

174827643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56395106-T-C

174828068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394677-C-T

174828423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394346-T-C

174828516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394254-G-T

174828590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394162-A-G

174828590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394162-A-T

174828624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394129-T-C

174828708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394045-A-G

174828708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394045-A-T

174828733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56394015-G-T

http://identifiers.org/hco/4/GRCh38#174829016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56393705-A-C

174829130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56393588-G-A

174829130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56393588-G-T

http://identifiers.org/hco/4/GRCh38#174829198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56393518-C-A

http://identifiers.org/hco/4/GRCh38#174829219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56393504-C-A

174829219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56393504-C-G

http://identifiers.org/hco/4/GRCh38#174829229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#56393494-C-A

174829229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56393494-C-T

174829235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4328
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56393488-T-C