66780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5 prime UTR variant
orthologous variants: 121450631-G-A

66780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5 prime UTR variant
orthologous variants: 121450631-G-C

66780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5 prime UTR variant
orthologous variants: 121450631-G-T

http://identifiers.org/hco/12/GRCh38#66785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121450626-A-C

66785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5 prime UTR variant
orthologous variants: 121450626-A-G

66785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5 prime UTR variant
orthologous variants: 121450626-A-T

67055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450348-A-G

67055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450348-A-T

67109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450291-T-C

67183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450220-T-C

67189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450214-G-A

67189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450214-G-C

67234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450184-G-A

67234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: stop_gained, undefined
orthologous variants: 121450184-G-T

http://identifiers.org/hco/12/GRCh38#67255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121450163-C-A

http://identifiers.org/hco/12/GRCh38#67258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121450160-C-A

67258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450160-C-T

http://identifiers.org/hco/12/GRCh38#67364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121450054-C-A

67364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450054-C-T

67369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450049-G-A

67369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, undefined
orthologous variants: 121450049-G-T

67869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121449569-G-A

67961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121449478-G-C

67961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121449478-G-T

68425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121449033-A-G

68610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448853-T-G

68686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448773-G-T

68717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448740-A-G

http://identifiers.org/hco/12/GRCh38#68845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121448591-A-C

68846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448590-G-A

68990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448486-T-A

http://identifiers.org/hco/12/GRCh38#69091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121448385-C-A

http://identifiers.org/hco/12/GRCh38#69344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121448128-C-A

69344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448128-C-T

69476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121448012-A-G

69832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447681-C-T

69963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447560-G-A

69974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447537-G-A

69974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447537-G-C

69974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447537-G-T

70121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447376-G-A

http://identifiers.org/hco/12/GRCh38#70167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121447331-C-A

70167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447331-C-T

70204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121447258-T-C

70807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121446679-T-C

71245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121446244-G-A

71444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121446052-G-C

71454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121446042-G-A

71454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121446042-G-T

71455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121446041-C-G

71503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445994-T-C

http://identifiers.org/hco/12/GRCh38#71515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121445982-C-A

71817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445749-C-T

71838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445728-C-T

71869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445690-G-A

71877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445683-G-A

72078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445502-A-G

72085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445495-C-T

72367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121445211-G-C

http://identifiers.org/hco/12/GRCh38#72743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121444844-A-C

72753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121444834-A-G

74189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121444089-A-G

http://identifiers.org/hco/12/GRCh38#74198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121444073-C-A

74302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121443956-G-A

74371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121443848-A-G

http://identifiers.org/hco/12/GRCh38#74554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121443648-C-A

74647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121443561-C-G

74664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121443545-G-A

74693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121443516-T-C

74986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121443141-T-G

75870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121442260-T-C

75953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121442189-G-A

75994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121442148-G-A

76411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441680-G-A

76411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441680-G-C

76567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441517-T-A

76573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441511-C-T

76786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441211-G-A

76795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441202-C-T

76964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441039-C-T

76966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121441037-A-G

77141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440875-G-A

77147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440869-G-A

77147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440869-G-C

http://identifiers.org/hco/12/GRCh38#77200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121440825-A-C

77200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440825-A-G

77244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440722-G-A

77244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440722-G-C

77244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440722-G-T

77286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440694-T-C

77308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121440672-A-G

77317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440663-A-G

77318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440662-A-G

77369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440619-T-C

77563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121440474-G-T

http://identifiers.org/hco/12/GRCh38#77573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121440464-C-A

77573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121440464-C-G

77573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121440464-C-T

77606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121440442-G-A

http://identifiers.org/hco/12/GRCh38#77626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121440424-C-A

77656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121440389-T-A

77696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121440348-G-T

http://identifiers.org/hco/12/GRCh38#77725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121440319-A-C

77737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121440299-G-A

77761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440274-G-A

77761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440274-G-T

77768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440267-C-T

77794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440224-C-T

77795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440223-G-A

http://identifiers.org/hco/12/GRCh38#77810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121440208-C-A

77810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121440208-C-T

77863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121440129-G-A

78016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121439992-G-A

78016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121439992-G-C

78146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121439878-C-G

http://identifiers.org/hco/12/GRCh38#78147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121439877-A-C

78147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121439877-A-G

78305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121439690-T-C

78569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121439326-T-C

78577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121439318-C-T

78608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121439293-G-A

78608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121439293-G-T

79261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438670-G-A

79261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438670-G-C

79368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438576-G-T

79747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438429-C-G

79810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438352-C-T

79817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438331-G-A

79914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438230-T-G

79941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438205-G-A

79947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121438199-T-A

80340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121437830-T-C

81211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121436996-A-G

81219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121436988-G-T

81227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121436983-C-T

81253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121436960-T-A

81732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121436149-C-G

81748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121436133-G-A

81947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121435919-G-C

82199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121435675-G-A

82199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121435675-G-T

82554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121435322-G-A

82565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121435311-C-T

83042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434866-C-T

83133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434804-G-A

http://identifiers.org/hco/12/GRCh38#83271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121434673-C-A

83271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434673-C-T

83295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434639-C-T

83375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434580-T-G

83404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434551-G-A

83462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434519-A-G

83677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434254-G-A

83677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434254-G-C

83694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434238-A-G

83927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121434067-C-G

84167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121433828-G-A

84627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121433434-G-T

84729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121433332-T-C

http://identifiers.org/hco/12/GRCh38#84918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121433124-C-A

85173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121432846-G-A

85356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121432667-A-G

85439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121432586-G-A

85532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121432510-C-T

85662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121432407-G-A

85871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121432223-G-T

88396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121429081-A-T

http://identifiers.org/hco/12/GRCh38#88678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121428832-C-A

88678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428832-C-T

88709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428802-T-G

88766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428754-C-T

88988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428629-A-G

88992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428625-C-T

89111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428493-T-C

89526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428094-C-T

89547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121428070-A-G

94442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425801-G-C

94637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425589-G-A

94637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425589-G-T

94638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425588-G-A

http://identifiers.org/hco/12/GRCh38#94727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121425503-C-A

94727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425503-C-T

94909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425368-A-G

94997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425280-C-T

95020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425257-C-T

http://identifiers.org/hco/12/GRCh38#95102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121425179-A-C

95105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121425176-T-A

95394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121424329-C-T

97877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121422350-A-G

97993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121422227-T-C

98029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121422191-G-T

98185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121422065-C-G

98267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421985-G-A

98267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421985-G-C

98547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421748-C-T

98588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421702-T-A

98588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421702-T-G

98838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421469-G-A

98858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421449-G-A

98858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421449-G-C

98970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421352-A-G

99104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421237-G-A

99119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421224-T-A

99119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421224-T-C

99119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121421224-T-G

http://identifiers.org/hco/12/GRCh38#99261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121421072-C-A

99261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121421072-C-T

99391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420956-A-G

99391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420956-A-T

99396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420951-G-A

99460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420889-T-C

99460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420889-T-G

99761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420599-T-A

99899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420472-C-T

100050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420364-T-C

100055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420359-T-A

100128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420302-G-A

100382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121420084-C-G

http://identifiers.org/hco/12/GRCh38#100620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121419814-A-C

100663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121419764-T-G

101118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121419383-G-A

101309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121419296-G-A

101501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121419142-T-G

101588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121419059-A-G

101653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121419009-A-T

101934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121418782-G-C

101957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121418758-A-G

102420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121418555-G-C

102934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121418139-C-T

102942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121418131-G-A

102958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121418112-C-T

103055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417986-A-G

103335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417699-G-A

104179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417537-T-C

104229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417511-A-G

http://identifiers.org/hco/12/GRCh38#104252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121417495-C-A

104310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417440-T-C

104514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417257-T-C

104570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417182-G-A

104570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121417182-G-C

105195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121416612-G-C

http://identifiers.org/hco/12/GRCh38#106656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121416158-C-A

106656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121416158-C-T

106679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121416135-T-C

106885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121415937-T-C

106968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121415833-G-T

106996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121415805-A-G

106999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121415802-G-T

114490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413707-G-A

114490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413707-G-C

114561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413651-G-A

114564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413648-A-T

114610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413606-A-G

114705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413500-A-G

114856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121413354-T-C

115447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121412155-T-G

117794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121411363-G-A

117885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121411277-G-A

118013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121411126-G-C

118101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121411054-A-G

118917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121410274-G-T

119594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409731-G-C

119633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409696-C-T

119649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409683-G-A

119662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409671-G-A

119690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409644-G-T

119781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409554-G-A

119867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121409470-G-C

120808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121408581-A-T

120990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121408425-G-A

121066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121408361-G-A

121066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121408361-G-T

121126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121408309-G-A

121463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121408019-C-T

http://identifiers.org/hco/12/GRCh38#122028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121407457-A-C

123592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406875-C-T

123669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406799-G-T

123723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406754-G-A

123723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406754-G-T

123886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406609-T-C

123937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406558-G-A

124503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406273-G-T

124522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406259-G-T

124593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406199-T-A

124609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406186-G-A

124779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406016-G-A

124779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121406016-G-T

125137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121405763-A-G

125149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121405751-G-A

125490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121405646-G-T

http://identifiers.org/hco/12/GRCh38#125573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121405582-C-A

125573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121405582-C-T

http://identifiers.org/hco/12/GRCh38#125822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121405344-C-A

125822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121405344-C-T

http://identifiers.org/hco/12/GRCh38#126039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121405149-C-A

126039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121405149-C-T

126108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121405072-G-T

126209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121404995-G-A

126626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121404744-T-C

126656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121404714-G-A

126715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121404674-C-T

126738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121404652-G-A

128016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402891-C-T

128383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402399-A-G

http://identifiers.org/hco/12/GRCh38#128413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121402369-C-A

128506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402275-T-C

128522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402263-T-C

128522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402263-T-G

128534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402251-A-G

128537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121402247-T-C

http://identifiers.org/hco/12/GRCh38#128712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121402105-A-C

http://identifiers.org/hco/12/GRCh38#128906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121401906-A-C

128964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401836-C-T

129085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401717-G-T

129173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401626-A-G

129230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401569-G-C

129326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401437-C-T

129448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401341-C-T

129658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121401115-T-C

129998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400775-T-G

130086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400689-C-G

130182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400602-G-C

130220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400562-G-C

131112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400102-C-T

131154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400061-G-A

131244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121400002-T-C

131252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399994-T-C

131312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399931-A-G

http://identifiers.org/hco/12/GRCh38#131342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121399901-C-A

131342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399901-C-T

131354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399886-G-A

131620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399593-A-G

131916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399360-C-T

132008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399275-G-A

132102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399198-C-G

132102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399198-C-T

132129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121399166-G-T

132594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398770-G-A

132594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398770-G-T

132736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398633-G-A

132740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398628-T-C

132780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398589-A-G

132849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398507-G-C

132881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398480-G-A

http://identifiers.org/hco/12/GRCh38#133184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121398231-C-A

133184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398231-C-G

133184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398231-C-T

133278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398132-G-A

133318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398089-T-G

133362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121398045-C-T

135307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121392872-T-G

135544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121393122-A-G

136850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121392170-G-A

138051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121390790-C-T

138136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121390711-A-G

138136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121390711-A-T

138333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121390507-A-G

138597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121390243-T-A

138798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121390048-G-A

138798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121390048-G-T

138897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389949-G-T

138919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389927-C-T

138921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389925-G-A

138941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121389905-G-A

138941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389905-G-T

138942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389904-G-A

138942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389904-G-C

138942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389904-G-T

138950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121389896-G-A

138994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389852-G-A

138994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389852-G-T

http://identifiers.org/hco/12/GRCh38#139060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121389756-C-A

139060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389756-C-G

139060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389756-C-T

139119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389703-G-A

139119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389703-G-T

139209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389610-T-C

139209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389610-T-G

139233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389586-G-A

139233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389586-G-C

139233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389586-G-T

http://identifiers.org/hco/12/GRCh38#139320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121389499-C-A

139320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121389499-C-T

http://identifiers.org/hco/12/GRCh38#139394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121389438-C-A

http://identifiers.org/hco/12/GRCh38#139395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121389437-C-A

139877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388860-A-G

139877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388860-A-T

http://identifiers.org/hco/12/GRCh38#139911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121388826-C-A

139911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388826-C-T

140077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388693-C-T

http://identifiers.org/hco/12/GRCh38#140164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121388623-C-A

140181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388606-C-T

140379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388453-A-G

http://identifiers.org/hco/12/GRCh38#140404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121388364-C-A

http://identifiers.org/hco/12/GRCh38#140561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121388226-C-A

140625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388162-T-C

140639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388148-A-G

140639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388148-A-T

140659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388143-G-C

140659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388143-G-T

140662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388140-C-T

http://identifiers.org/hco/12/GRCh38#140672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121388131-C-A

140720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388094-G-A

140720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388094-G-T

http://identifiers.org/hco/12/GRCh38#140764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121388071-C-A

140764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388071-C-G

140764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121388071-C-T

140838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388050-G-A

140838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388050-G-T

140881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388016-G-C

140881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121388016-G-T

140914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 121387949-T-G

http://identifiers.org/hco/12/GRCh38#140937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121387926-C-A

140937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387926-C-T

140981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387877-T-A

140981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387877-T-C

140981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387877-T-G

http://identifiers.org/hco/12/GRCh38#141002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121387856-C-A

141002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387856-C-T

141017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387839-G-T

141053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387802-A-G

http://identifiers.org/hco/12/GRCh38#141062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121387793-A-C

141197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121387659-T-G

141200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121387656-C-T

141209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 121387647-C-T

141275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121387581-G-A

141275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121387581-G-C

141303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121387555-C-T

141311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121387547-C-G

141311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121387547-C-T

141507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387425-T-A

141507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387425-T-C

141518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387414-A-G

141633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387318-G-A

141633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387318-G-T

http://identifiers.org/hco/12/GRCh38#141696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121387239-C-A

141696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387239-C-T

http://identifiers.org/hco/12/GRCh38#141809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121387134-C-A

141809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387134-C-G

141809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387134-C-T

http://identifiers.org/hco/12/GRCh38#141810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121387133-C-A

141810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387133-C-G

141844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387101-T-A

141844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387101-T-C

141844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121387101-T-G

141994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386996-G-A

142190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386926-G-T

142209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386907-C-T

142238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386881-G-A

142238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386881-G-C

142295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386838-G-A

142295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386838-G-T

142302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121386831-T-C

http://identifiers.org/hco/12/GRCh38#142517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121386548-C-A

142804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386294-G-A

142845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386256-G-A

142904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386198-C-G

142904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386198-C-T

143022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386060-C-T

143052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386031-T-C

143077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121386007-C-T

143124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385975-T-C

143137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385962-T-C

http://identifiers.org/hco/12/GRCh38#143147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121385952-C-A

143147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385952-C-T

143154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385937-G-T

143163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385931-G-A

143163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385931-G-T

143181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121385915-T-C

http://identifiers.org/hco/12/GRCh38#143246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121385845-A-C

143246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121385845-A-G

143308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121385796-A-G

http://identifiers.org/hco/12/GRCh38#143385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121385726-C-A

http://identifiers.org/hco/12/GRCh38#143410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121385702-C-A

143410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 121385702-C-T

143445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385667-A-G

143561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385540-G-T

143562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385539-G-A

143773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385466-A-G

143773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385466-A-T

143782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385457-G-A

143782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385457-G-T

143818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385424-T-C

143818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385424-T-G

143880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385393-T-C

143907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385366-A-G

143949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385332-G-C

143958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385323-G-A

143958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385323-G-T

144042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121385242-A-G

144045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121385239-C-G

http://identifiers.org/hco/12/GRCh38#144083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121385169-C-A

144083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121385169-C-T

144161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385097-A-G

144219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385039-G-A

144219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385039-G-T

144240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121385015-G-T

144284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121384942-C-G

144284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121384942-C-T

http://identifiers.org/hco/12/GRCh38#144314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121384914-C-A

144314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384914-C-T

144334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384894-A-G

144348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384880-T-C

144373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384848-T-A

144373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384848-T-C

http://identifiers.org/hco/12/GRCh38#144416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121384805-C-A

144416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384805-C-T

144507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384715-G-A

144507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121384715-G-T

145496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121382848-T-C

145629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121382706-C-G

145642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121382693-G-A

145642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121382693-G-C

145821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121382508-G-A

145935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121382391-G-A

145935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121382391-G-T

145986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121382339-T-A

146336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121381993-G-A

146869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121381520-G-A

147009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121381404-G-A

147183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121381245-C-T

147240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121381197-G-T

http://identifiers.org/hco/12/GRCh38#147831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121380736-C-A

http://identifiers.org/hco/12/GRCh38#147890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121380681-C-A

147890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380681-C-T

http://identifiers.org/hco/12/GRCh38#147905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121380666-C-A

147908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380663-A-G

147908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380663-A-T

http://identifiers.org/hco/12/GRCh38#147953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121380600-C-A

147954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380599-C-T

148053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380488-A-T

148213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380296-G-A

148213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380296-G-T

148400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121380134-G-A

148550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121379995-A-G

148610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121379936-G-A

148610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121379936-G-C

148610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121379936-G-T

148745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121379804-C-T

149032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121379524-T-A

http://identifiers.org/hco/12/GRCh38#149038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121379518-C-A

http://identifiers.org/hco/12/GRCh38#149189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121379356-C-A

149189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121379356-C-T

http://identifiers.org/hco/12/GRCh38#149205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121379332-C-A

149236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121379299-A-G

149642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121378904-C-T

149876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121378766-G-A

149993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121378665-C-G

150278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121378413-C-G

152900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121371332-A-T

152998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121371241-C-G

152998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121371241-C-T

153111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121371141-C-T

153375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121370900-C-G

153528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, undefined
orthologous variants: 121370679-C-T

153757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121370302-G-C

154160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121369928-C-T

154348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121369738-C-G

154728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121369333-C-T

154887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121369185-T-C

154978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121369084-C-T

155156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121368928-G-A

155741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121368449-G-C

155881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121368284-G-T

156039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121368116-G-A

156110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121368047-A-G

156119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121368038-G-C

156805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121367377-C-T

156888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121367254-T-C

156888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121367254-T-G

156971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121367126-T-C

http://identifiers.org/hco/12/GRCh38#157001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121367109-C-A

157001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121367109-C-T

157113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: 121366991-G-T

http://identifiers.org/hco/12/GRCh38#157154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121366949-C-A

157154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121366949-C-T

http://identifiers.org/hco/12/GRCh38#157161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121366942-C-A

157161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366942-C-T

http://identifiers.org/hco/12/GRCh38#157211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121366908-A-C

157211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366908-A-G

157211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366908-A-T

157252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366858-G-T

http://identifiers.org/hco/12/GRCh38#157255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121366848-C-A

157255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366848-C-T

157286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366818-G-A

157286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366818-G-T

157390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366680-T-A

157390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366680-T-G

http://identifiers.org/hco/12/GRCh38#157418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121366653-C-A

157701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121366417-A-G

157701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121366417-A-T

157719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366401-G-A

http://identifiers.org/hco/12/GRCh38#157754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121366359-C-A

157767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366346-G-A

157767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366346-G-C

157767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366346-G-T

157786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366327-A-G

157809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366304-G-A

157809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366304-G-T

157812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366301-T-C

157833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366280-G-A

157833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366280-G-T

157974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121366148-A-G

http://identifiers.org/hco/12/GRCh38#161816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121364914-C-A

161816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364914-C-T

http://identifiers.org/hco/12/GRCh38#161819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121364911-C-A

161819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364911-C-T

http://identifiers.org/hco/12/GRCh38#161824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121364906-C-A

161824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364906-C-G

161824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364906-C-T

161842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364883-T-A

161842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364883-T-C

161842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364883-T-G

161999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: synonymous variant
orthologous variants: 121364757-C-G

http://identifiers.org/hco/12/GRCh38#162084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121364633-C-A

162084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364633-C-G

162084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364633-C-T

http://identifiers.org/hco/12/GRCh38#162198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121364553-C-A

162198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364553-C-G

162198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364553-C-T

162432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364346-C-T

162736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121364104-T-C

163101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363807-G-A

http://identifiers.org/hco/12/GRCh38#163230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121363749-C-A

163429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363724-G-C

163454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363696-G-A

163454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363696-G-C

http://identifiers.org/hco/12/GRCh38#163467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121363683-C-A

163467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363683-C-G

163478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363672-C-T

http://identifiers.org/hco/12/GRCh38#163506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121363643-C-A

163506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: 121363643-C-T

163512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: 121363637-C-T

163548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: 121363601-A-G

http://identifiers.org/hco/12/GRCh38#163557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121363592-A-C

163612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: 121363537-T-G

http://identifiers.org/hco/12/GRCh38#163614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121363535-C-A

163614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: synonymous variant
orthologous variants: 121363535-C-T

163646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363505-G-A

http://identifiers.org/hco/12/GRCh38#163658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121363493-C-A

163658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363493-C-T

163725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363432-T-C

163779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363411-C-T

163921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363295-A-T

163928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121363288-G-A

164517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121362234-C-T

http://identifiers.org/hco/12/GRCh38#164535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121362197-C-A

164535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121362197-C-T

164619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121362093-G-A

164619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron variant
orthologous variants: 121362093-G-C

164635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121362078-G-T

164828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121361856-G-A

165057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121361616-G-A

165060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121361613-A-G

http://identifiers.org/hco/12/GRCh38#165167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121361514-C-A

http://identifiers.org/hco/12/GRCh38#165197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121361484-C-A

165254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121361445-T-G

165263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121361436-G-T

165328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121361344-A-G

165348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121361329-G-A

165348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121361329-G-T

http://identifiers.org/hco/12/GRCh38#165395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121361291-C-A

165395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121361291-C-T

165635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121361121-G-A

165635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121361121-G-T

165851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121360911-A-G

166850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360617-T-C

166873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360595-T-C

167117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360356-T-C

167132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360339-A-T

167151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360320-A-G

167320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360154-C-T

167322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121360152-A-G

167505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121359956-G-T

167516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121359945-A-G

167546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121359912-G-T

167598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121359857-G-A

167618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 121359835-A-G

168008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121359539-T-G

168016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121359531-C-T

168662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358999-G-A

168663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358998-A-G

http://identifiers.org/hco/12/GRCh38#168915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121358786-C-A

168915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358786-C-T

169036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121358675-A-G

169226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358541-G-A

169226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358541-G-T

169276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358531-G-A

169736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358233-G-C

169903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358093-G-A

169980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358036-T-C

169991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121358026-T-C

170572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121357549-C-T

170645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121357483-A-T

170974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121357176-G-A

170974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121357176-G-T

171141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121356972-C-T

171329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121356784-A-G

171661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121356439-G-A

171818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121356292-G-A

172588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355656-A-G

172733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355524-C-T

172959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355378-G-T

172993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355341-C-G

http://identifiers.org/hco/12/GRCh38#173015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121355319-A-C

173219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355128-G-C

173267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355085-C-T

173291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121355062-G-A

173372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121354988-G-T

173550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121354824-C-T

174123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353826-A-T

174429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353640-G-A

174469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353613-G-A

174469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353613-G-C

174469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353613-G-T

http://identifiers.org/hco/12/GRCh38#174476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121353606-C-A

174476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353606-C-G

174476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353606-C-T

http://identifiers.org/hco/12/GRCh38#174478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121353604-A-C

174478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353604-A-G

174478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121353604-A-T

174725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121353335-C-T

http://identifiers.org/hco/12/GRCh38#174740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121353320-C-A

174740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121353320-C-G

174740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121353320-C-T

http://identifiers.org/hco/12/GRCh38#175017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#121353043-C-A

175017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121353043-C-T

http://identifiers.org/hco/12/GRCh38#175091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352970-C-A

175091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352970-C-G

175091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352970-C-T

175130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352932-T-A

175146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352919-T-A

175146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352919-T-G

http://identifiers.org/hco/12/GRCh38#175170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352900-C-A

http://identifiers.org/hco/12/GRCh38#175252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352816-C-A

175252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121352816-C-T

175336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121352736-A-G

175386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121352678-G-A

175386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121352678-G-T

175456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352617-G-A

http://identifiers.org/hco/12/GRCh38#175517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352557-C-A

175517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121352557-C-T

175526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121352546-A-G

175526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121352546-A-T

http://identifiers.org/hco/12/GRCh38#175561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352514-C-A

175561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352514-C-T

http://identifiers.org/hco/12/GRCh38#175566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352509-A-C

175566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352509-A-G

175566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352509-A-T

175627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352449-T-C

175627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352449-T-G

http://identifiers.org/hco/12/GRCh38#175715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352387-C-A

175715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352387-C-T

175733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352374-C-T

175800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352309-T-C

http://identifiers.org/hco/12/GRCh38#175870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352241-C-A

175870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352241-C-T

http://identifiers.org/hco/12/GRCh38#175933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121352176-C-A

175933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352176-C-T

175944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352164-C-T

175947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352161-G-A

175947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352161-G-T

176004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352137-G-T

176021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352120-A-G

176025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121352116-G-T

176295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351889-G-A

176295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351889-G-T

http://identifiers.org/hco/12/GRCh38#176338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351865-C-A

176338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351865-C-T

176340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351863-G-A

176340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351863-G-T

176353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351850-G-T

176354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351849-G-A

176354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351849-G-T

http://identifiers.org/hco/12/GRCh38#176355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351848-C-A

http://identifiers.org/hco/12/GRCh38#176356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351847-C-A

176382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351820-T-A

http://identifiers.org/hco/12/GRCh38#176413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351787-C-A

http://identifiers.org/hco/12/GRCh38#176427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351773-C-A

176535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351654-C-T

176614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351569-T-C

http://identifiers.org/hco/12/GRCh38#176641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351439-C-A

http://identifiers.org/hco/12/GRCh38#176708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351392-C-A

176739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351361-T-A

176739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351361-T-C

http://identifiers.org/hco/12/GRCh38#176744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351356-C-A

176744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351356-C-T

http://identifiers.org/hco/12/GRCh38#176759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351343-C-A

176759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121351343-C-T

http://identifiers.org/hco/12/GRCh38#176812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351297-C-A

176919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351216-G-T

176934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351202-G-C

176934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351202-G-T

176943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351193-A-G

http://identifiers.org/hco/12/GRCh38#176978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121351161-C-A

177093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351049-G-A

177093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121351049-G-T

177233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350998-G-A

177233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350998-G-T

177242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350989-C-G

http://identifiers.org/hco/12/GRCh38#177407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121350907-C-A

177457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350852-A-G

http://identifiers.org/hco/12/GRCh38#177471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121350840-C-A

177666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350655-T-C

177666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350655-T-G

http://identifiers.org/hco/12/GRCh38#177703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121350625-C-A

http://identifiers.org/hco/12/GRCh38#177717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121350611-C-A

177742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350586-T-C

http://identifiers.org/hco/12/GRCh38#177745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121350583-A-C

177745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350583-A-G

177795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350548-T-C

177796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350547-C-T

177817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350538-G-A

177817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350538-G-T

177821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350534-A-G

177829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350526-C-T

177899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350455-G-A

http://identifiers.org/hco/12/GRCh38#177925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121350424-C-A

177925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121350424-C-T

178128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121350227-T-C

178193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121350150-G-A

178193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121350150-G-T

178211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121350132-C-T

178260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121350084-T-C