168079674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165154182-T-G

168079821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165154045-T-G

168079889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165153987-T-C

168079915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165153962-A-G

http://identifiers.org/hco/1/GRCh38#168079956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153921-C-A

168080167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165153766-T-C

168080272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153721-C-T

168080304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153684-G-A

http://identifiers.org/hco/1/GRCh38#168080326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153668-C-A

http://identifiers.org/hco/1/GRCh38#168080350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153644-C-A

http://identifiers.org/hco/1/GRCh38#168080391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153612-C-A

168080391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153612-C-T

168080408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153589-G-A

168080447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153549-G-T

168080637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153359-A-G

168080637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153359-A-T

168080660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153341-G-T

http://identifiers.org/hco/1/GRCh38#168080692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153307-C-A

168080692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153307-C-G

http://identifiers.org/hco/1/GRCh38#168080762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153240-C-A

168080762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153240-C-T

168080805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153220-A-G

168080814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153211-A-G

http://identifiers.org/hco/1/GRCh38#168080847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165153178-C-A

168080847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153178-C-T

168080853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153172-G-A

168080853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153172-G-T

168080863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153162-T-C

168081254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153098-T-C

168081318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165153042-T-C

168081524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165152841-G-A

168081524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165152841-G-T

168081535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152830-G-A

168081550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152815-A-G

168081599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165152768-T-C

168081658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152721-T-C

168081759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152632-A-G

168081818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152575-C-T

http://identifiers.org/hco/1/GRCh38#168081827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165152564-C-A

168081827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152564-C-G

168081827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152564-C-T

168081948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165152462-A-G

168082001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152408-T-C

168082166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152250-A-G

168082249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152200-A-G

168082282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165152156-T-C

http://identifiers.org/hco/1/GRCh38#168082283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165152155-C-A

168082292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152146-A-G

168082305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152132-A-G

168082305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152132-A-T

168082323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152112-A-G

168082323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165152112-A-T

http://identifiers.org/hco/1/GRCh38#168082422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165152025-A-C

168082422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165152025-A-G

http://identifiers.org/hco/1/GRCh38#168082498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151948-C-A

168082498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151948-C-T

http://identifiers.org/hco/1/GRCh38#168082554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151897-C-A

168082554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151897-C-T

http://identifiers.org/hco/1/GRCh38#168082559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151892-C-A

168082581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151870-G-T

http://identifiers.org/hco/1/GRCh38#168082711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151745-C-A

168082741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151717-T-A

168082779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151682-G-A

168082779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151682-G-T

168082830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151626-G-A

168082830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151626-G-T

http://identifiers.org/hco/1/GRCh38#168082848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151608-C-A

168082848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151608-C-T

168082882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151580-T-C

168082961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151512-G-T

168082968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151505-G-T

168082975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151498-A-G

168082988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151486-A-T

168083013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151461-C-T

168083055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151420-C-T

http://identifiers.org/hco/1/GRCh38#168083067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151409-C-A

http://identifiers.org/hco/1/GRCh38#168083098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151392-C-A

168083098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151392-C-T

168083100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151390-A-G

http://identifiers.org/hco/1/GRCh38#168083127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151366-C-A

168083129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151364-G-A

168083129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151364-G-T

http://identifiers.org/hco/1/GRCh38#168083249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151258-A-C

168083273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151242-G-A

168083273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151242-G-T

http://identifiers.org/hco/1/GRCh38#168083370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151181-C-A

http://identifiers.org/hco/1/GRCh38#168083467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165151102-C-A

168083558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151024-G-A

168083558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151024-G-T

168083568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165151014-A-T

168083601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150986-A-G

168083721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150942-C-T

168083732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150931-G-T

168083756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150904-G-A

168083773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150890-C-T

http://identifiers.org/hco/1/GRCh38#168084169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165150569-C-A

http://identifiers.org/hco/1/GRCh38#168084188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165150550-C-A

168084222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150517-G-T

168084245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150478-T-C

168084314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150416-T-G

http://identifiers.org/hco/1/GRCh38#168084341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165150389-C-A

168084459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150272-A-G

168084463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150268-G-T

168084623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165150121-T-C

168084884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149897-G-C

http://identifiers.org/hco/1/GRCh38#168084962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165149788-C-A

168084962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149788-C-T

168085011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149734-A-T

168085019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149726-C-T

168085045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149701-A-G

168085092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149656-C-T

168085183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149568-G-T

http://identifiers.org/hco/1/GRCh38#168085197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165149553-C-A

168085197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149553-C-T

168085203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149547-G-A

168085203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149547-G-T

http://identifiers.org/hco/1/GRCh38#168085234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165149532-A-C

168085264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149502-T-G

168085265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3 prime UTR variant
orthologous variants: 165149501-T-G

168085281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 165149492-T-G

168085293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 165149482-G-A

168085293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 165149482-G-T

168085395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 165149384-T-C

http://identifiers.org/hco/1/GRCh38#168085511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165149288-C-A

168085511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 165149288-C-T

168085524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 165149275-G-C

168085556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165149243-T-C

168085627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 165149172-G-A

168085724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 165149075-A-T

168085804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 165148995-A-G

168085891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165148931-G-A

168085891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165148931-G-T

168085933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165148887-T-A

168086293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165148606-C-G

168086293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165148606-C-T

168086333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165148565-C-T

http://identifiers.org/hco/1/GRCh38#168086688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165148233-A-C

http://identifiers.org/hco/1/GRCh38#168086713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165148209-A-C

168087276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165147739-A-G

168087331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165146655-G-C

http://identifiers.org/hco/1/GRCh38#168087470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165146528-A-C

168087472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165146526-G-A

168087472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165146526-G-T

168087723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146300-T-C

168087723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146300-T-G

168087736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146287-C-G

168087736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146287-C-T

168087756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146275-G-T

168087771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146260-C-T

http://identifiers.org/hco/1/GRCh38#168087780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165146252-C-A

168087780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146252-C-T

168087796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146238-T-C

168087800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146234-G-A

168087800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146234-G-T

168087821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146213-A-G

168087892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165146141-G-A

168090202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165145284-G-A

168090298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165145168-A-T

168090379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165145092-G-C

168090379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165145092-G-T

http://identifiers.org/hco/1/GRCh38#168090447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165145024-A-C

168090447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165145024-A-G

168090452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165145019-G-A

168090452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165145019-G-T

http://identifiers.org/hco/1/GRCh38#168090470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165145009-A-C

168090557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 165144921-A-G

168090593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165144882-T-C

168090596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165144879-C-G

http://identifiers.org/hco/1/GRCh38#168090647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165144828-A-C

http://identifiers.org/hco/1/GRCh38#168090737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165144736-C-A

168090737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144736-C-G

168090909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144593-C-T

168091077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144466-C-T

168091140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144437-C-G

168091140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144437-C-T

168091219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144356-G-A

168091294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144258-G-A

168091511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165144113-G-A

168092157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165142452-G-A

168092157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165142452-G-C

168092233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165142390-C-G

168092278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165142344-C-T

http://identifiers.org/hco/1/GRCh38#168092320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165142305-C-A

168092461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165142208-A-G

168092615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165142065-G-C

168092830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165141838-T-C

168092946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165141741-G-A

168093493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165141309-C-T

168093744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165141032-C-G

168093776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165141011-G-A

168093945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165140820-C-T

168094149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165140655-T-C

168094474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165140334-C-T

168094590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165140222-G-A

168094861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139977-T-A

168094913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139919-C-T

http://identifiers.org/hco/1/GRCh38#168094916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165139916-A-C

168094916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139916-A-G

168094916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139916-A-T

http://identifiers.org/hco/1/GRCh38#168094959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165139876-C-A

168094959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139876-C-T

168095024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139816-C-G

168095079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139762-A-T

168095575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139413-T-C

168095659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139247-C-T

http://identifiers.org/hco/1/GRCh38#168095669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165139237-C-A

168095676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139230-G-T

168095739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139149-G-C

168095862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165139037-T-C

168095931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138979-T-C

168096132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138914-T-A

168096132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138914-T-C

168096132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138914-T-G

168096315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138739-G-A

168096315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138739-G-C

168096382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138672-G-C

168096382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138672-G-T

168096389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138665-G-A

168096389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165138665-G-T

168097209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 165137859-A-G

168097252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165137817-A-T

http://identifiers.org/hco/1/GRCh38#168102212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165136653-C-A

168102341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165136547-T-C

168102341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165136547-T-G

168102351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165136537-G-A

168102631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165136337-T-A

168102631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165136337-T-C

168102950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165136054-A-G

168103887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134845-C-T

168103888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134844-G-A

168104049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134688-G-C

168104135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134588-G-A

http://identifiers.org/hco/1/GRCh38#168104300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165134322-C-A

http://identifiers.org/hco/1/GRCh38#168104332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165134290-C-A

168104332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134290-C-T

168104431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134206-C-T

http://identifiers.org/hco/1/GRCh38#168104438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165134199-C-A

168104444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165134193-T-A

168104567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165134069-A-G

168104729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165133907-A-G

168104925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133716-G-A

168104925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133716-G-T

168104928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133713-A-G

http://identifiers.org/hco/1/GRCh38#168104944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165133697-C-A

168104944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133697-C-T

168104945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133696-A-G

168104945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133696-A-T

168104962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133679-G-T

http://identifiers.org/hco/1/GRCh38#168105025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165133611-C-A

168105025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133611-C-T

http://identifiers.org/hco/1/GRCh38#168105036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165133597-C-A

168105036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133597-C-T

168105037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133596-A-G

168105396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133153-A-G

168105481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165133081-C-T

168105904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165132636-G-A

168106677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165132103-T-C

168106687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165132093-T-G

168106864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165131924-T-C

168107015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165131759-C-T

168113564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165130239-T-C

168114659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165129859-T-A

168114659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165129859-T-C

http://identifiers.org/hco/1/GRCh38#168114670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165129848-C-A

http://identifiers.org/hco/1/GRCh38#168115173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165129399-C-A

168115234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165129330-G-A

168116300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165128179-G-A

168116344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165128139-T-G

168116677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165127821-T-C

http://identifiers.org/hco/1/GRCh38#168116742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165127755-A-C

168117075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165127470-T-C

168117724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165127166-G-T

168117855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165127035-C-T

168117857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165127033-C-T

168117895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165126995-G-C

168118098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165126774-C-T

168118148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165126683-A-T

168121799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165123932-G-A

168121988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165123776-G-A

168121990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165123774-G-A

168122185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165123585-C-T

168122190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165123580-C-T

168123788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165122194-A-G

168123898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165122150-C-T

168123918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165122130-T-C

168123940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165122110-G-C

168124104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165121972-T-C

168124105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165121971-C-G

168124203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165121876-A-G

168124719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165121056-G-C

168124740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165121026-G-A

168124757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165121005-G-A

168124775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165120989-G-A

168125158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165120605-T-C

168125246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165120518-C-T

168125447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165120289-C-T

168125766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165119867-C-T

168126672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165119027-T-A

168126748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165118933-C-T

168127973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117902-T-C

168127974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117901-A-G

168128038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117838-G-A

168128197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117709-C-T

168128353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117566-T-A

168128384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117533-G-A

168128435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165117495-C-G

168130934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165116324-T-C

168131266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165115919-T-C

168131341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165115845-T-C

168131442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165115752-T-C

168131537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165115665-G-T

168131742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114482-C-T

168131745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114479-C-G

168131863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114344-T-C

168131887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114316-T-A

168131887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114316-T-C

168131970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114225-A-G

168131978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114217-T-A

168133128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165114038-A-G

168133757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165113198-A-G

168133758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165113197-G-C

168133758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165113197-G-T

168134118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111915-G-T

168134180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111862-C-T

168134293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111759-T-C

168134348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111698-G-C

168134798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111519-G-A

168134798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111519-G-T

168134802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111515-A-G

168134803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111514-G-A

168134803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111514-G-C

168134803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111514-G-T

http://identifiers.org/hco/1/GRCh38#168134804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165111513-C-A

168134804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111513-C-T

168134843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111488-T-C

168134849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111482-A-G

168134849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111482-A-T

168134850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165111481-C-G

168134927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165111417-T-A

168134927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165111417-T-C

168135039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165111329-G-A

168135060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165111316-G-C

168135133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165111243-G-T

http://identifiers.org/hco/1/GRCh38#168135306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165110969-C-A

168135368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165110899-A-G

168135531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165110771-C-T

168135565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165110737-C-T

168135624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165110674-A-G

168135925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, undefined
orthologous variants: 165110455-G-T

http://identifiers.org/hco/1/GRCh38#168135981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165110401-C-A

168135981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, undefined
orthologous variants: 165110401-C-G

http://identifiers.org/hco/1/GRCh38#168136054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165110334-C-A

168136054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165110334-C-T

168136063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 165110324-A-G

168136172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 165110223-G-A

168136172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 165110223-G-C

168136187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 165110208-G-A

168136187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 165110208-G-T

168136245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165110156-A-G

168136248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165110153-G-A

168136248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165110153-G-C

168136248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165110153-G-T

http://identifiers.org/hco/1/GRCh38#168136277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165110124-C-A

168136277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 165110124-C-G

168136277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 165110124-C-T

168136412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165110005-G-T

168136430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109995-G-A

168136430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109995-G-C

168136476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109949-A-G

http://identifiers.org/hco/1/GRCh38#168136577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165109824-A-C

168136577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 165109824-A-G

168136754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109630-G-C

168136754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109630-G-T

168136777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109612-G-A

168136777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109612-G-T

168136839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109569-T-A

168136839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109569-T-C

168136839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109569-T-G

http://identifiers.org/hco/1/GRCh38#168137020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165109394-C-A

168137020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109394-C-T

168137095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109336-C-T

168137112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109319-T-C

168137112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109319-T-G

http://identifiers.org/hco/1/GRCh38#168137116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165109315-A-C

168137135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109287-C-G

168137135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109287-C-T

168137155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron variant
orthologous variants: 165109254-T-C

http://identifiers.org/hco/1/GRCh38#168137163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165109247-A-C

168137163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: intron_variant, undefined
orthologous variants: 165109247-A-G

168137169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109241-T-C

168137184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109227-T-C

168137345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109088-T-C

168137357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109076-G-A

168137357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165109076-G-T

168137428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5 prime UTR variant
orthologous variants: 165109015-G-T

168137496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 165108931-G-T

168137521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5 prime UTR variant
orthologous variants: 165108906-T-A

http://identifiers.org/hco/1/GRCh38#168137548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165108880-C-A

168137548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5 prime UTR variant
orthologous variants: 165108880-C-T

168137612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5 prime UTR variant
orthologous variants: 165108829-C-T

168137623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23694
most severe consequence: 5 prime UTR variant
orthologous variants: 165108818-C-T