http://identifiers.org/hco/9/GRCh38#134641815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#27776474-C-A

134641815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27776474-C-G

134641815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27776474-C-T

http://identifiers.org/hco/9/GRCh38#134642016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27776665-C-A

134642016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: 27776665-C-T

http://identifiers.org/hco/9/GRCh38#134642029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27776678-C-A

134642029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: 27776678-C-T

http://identifiers.org/hco/9/GRCh38#134642048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27776697-C-A

134642048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: 27776697-C-T

134642088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: 27776738-G-A

134642088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5 prime UTR variant
orthologous variants: 27776738-G-T

134642117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27776767-T-C

http://identifiers.org/hco/9/GRCh38#134642687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27777333-C-A

134642687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27777333-C-G

134643383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27777961-C-T

134643433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778011-T-C

134643629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778190-G-C

134643746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778285-G-A

134643806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778330-T-A

134643842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778366-C-T

134644105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778641-G-A

134644105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778641-G-C

134644117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778653-C-T

134644153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778691-T-C

134644613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27778761-C-T

134644908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779051-A-G

134644978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779126-C-T

134645140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27779317-G-T

134645167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779343-G-A

134645203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779380-C-T

http://identifiers.org/hco/9/GRCh38#134645230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27779408-C-A

134645275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779456-C-T

134645499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779646-G-A

134645582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27779724-A-T

134645788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27779835-C-T

134646031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780052-C-G

134646194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780201-G-T

134646415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780349-G-C

134646480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780396-G-A

134646530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780450-C-G

134646531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780451-A-G

134646635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780573-G-A

134646635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780573-G-T

134646707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780628-A-G

134646841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780705-C-T

134646991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780860-C-T

http://identifiers.org/hco/9/GRCh38#134647007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27780871-C-A

134647061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27780911-C-T

134647191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781021-C-T

134647217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781043-T-C

134647289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781096-C-T

134647377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781171-G-A

134647484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781271-T-C

134647523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781304-A-G

134647525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781306-A-G

134647579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781316-T-C

134647640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781363-A-G

134647760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781468-T-C

134647762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27781470-T-C

134650645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27783712-C-T

134650651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27783718-C-T

134655327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27785153-G-T

134655680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27785665-G-A

134655680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27785665-G-C

134655798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27785789-G-A

134655798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27785789-G-C

134656067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27786039-G-T

134656282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27786229-C-G

http://identifiers.org/hco/9/GRCh38#134656409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27786330-A-C

134656493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27786414-A-G

134657817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27786848-C-T

134657922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27786947-G-A

http://identifiers.org/hco/9/GRCh38#134657996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27786962-C-A

134658202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787142-C-G

134658202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787142-C-T

134658700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787616-C-T

134658795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787740-G-C

http://identifiers.org/hco/9/GRCh38#134658832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27787777-A-C

134658832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787777-A-G

134658907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787829-G-A

134658924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27787840-C-T

134659560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789279-G-A

134659657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789345-G-A

134659767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789438-C-G

134659767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789438-C-T

134659775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789448-G-A

http://identifiers.org/hco/9/GRCh38#134659938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27789594-A-C

134660004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789718-C-T

134660098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27789815-C-T

134660604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27790119-T-C

134660774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27790237-G-A

134660928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27790384-G-C

134661293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27790663-A-T

134661295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27790665-C-T

134661325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27790694-C-T

134661727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791277-C-T

134661805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791342-C-T

http://identifiers.org/hco/9/GRCh38#134661834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27791376-C-A

134662055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791511-T-C

134662117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791557-T-A

134662189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791618-C-G

134662272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791697-G-A

134662306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791732-C-T

134662379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791797-C-T

134662380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27791798-G-A

http://identifiers.org/hco/9/GRCh38#134662489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27791887-C-A

134662627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792048-G-T

134662637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792058-C-G

134662651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792072-C-T

134662656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792077-C-T

134662728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792152-T-G

134662811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792204-C-T

134662844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792237-T-C

134662907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792303-T-A

134662909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792305-G-A

134662909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792305-G-C

134662972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792348-G-A

134663124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792471-T-C

134663143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27792486-C-G

134663972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27793264-A-G

134663995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27793286-G-C

134664028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27793315-G-C

134664040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27793331-G-C

134664108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27793400-T-C

134664329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27793644-A-G

134665284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794163-T-C

134665339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794222-G-A

134665361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794251-G-T

134665453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794345-G-A

134665538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794433-G-T

134665826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794883-G-A

134665826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794883-G-C

134665826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794883-G-T

134665863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794919-G-A

134665871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27794932-T-C

134666086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27795172-C-T

134666087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27795173-G-A

134666198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27795282-G-A

134666367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27795405-C-T

134666383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27795422-A-G

134666406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27795445-G-T

134670208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27795848-G-A

134670340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27795975-T-G

134670462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27796102-C-T

134670463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27796103-C-T

134670596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27796358-C-T

134671427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797123-G-A

134671609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797353-G-A

134671741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797510-C-T

134671850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797619-C-T

http://identifiers.org/hco/9/GRCh38#134672089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27797849-C-A

134672089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797849-C-G

134672138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797899-T-C

134672207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27797960-T-C

134672504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798491-G-A

134672504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798491-G-C

134672504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798491-G-T

134672614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798582-G-A

134672614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798582-G-C

134672653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798614-A-G

134672740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798700-G-A

134672834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798793-G-T

134672906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27798861-G-A

134680801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806306-A-T

134681062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806535-G-A

134681103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806575-C-T

134681506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806822-T-C

134681537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806839-G-A

134681538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806840-C-T

134681658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806887-G-C

134681761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806949-C-T

134681783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27806970-G-T

http://identifiers.org/hco/9/GRCh38#134681808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27807001-A-C

134681808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807001-A-G

134681855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807054-T-G

134681870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807067-G-A

134681883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807080-T-A

http://identifiers.org/hco/9/GRCh38#134681887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27807084-C-A

134681887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807084-C-G

134681926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807123-T-G

134683710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807894-C-T

134683764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27807939-T-C

http://identifiers.org/hco/9/GRCh38#134683790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27807967-C-A

134683835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808008-T-C

134683839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808012-C-G

134684024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808175-C-T

http://identifiers.org/hco/9/GRCh38#134684166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27808308-C-A

134684166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808308-C-T

134684357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808459-C-G

134684366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808466-G-A

134684472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27808552-T-C

http://identifiers.org/hco/9/GRCh38#134687669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27809195-C-A

134687669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809195-C-T

134687673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809199-C-T

http://identifiers.org/hco/9/GRCh38#134687732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27809258-C-A

134687732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809258-C-T

134687943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809440-C-T

134688095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809619-G-A

134688200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809723-C-T

134688275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809795-G-A

134688275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809795-G-C

http://identifiers.org/hco/9/GRCh38#134688304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27809827-C-A

134688379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809900-C-G

134688379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27809900-C-T

134690785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27811913-G-T

134690830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27811941-T-C

http://identifiers.org/hco/9/GRCh38#134690833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27811944-C-A

134690833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27811944-C-G

134690860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27811973-A-G

134690894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812014-C-T

134691042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27812159-C-T

134691087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 27812204-C-G

134691087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 27812204-C-T

134691135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812253-C-T

134691136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812254-A-G

http://identifiers.org/hco/9/GRCh38#134691178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27812304-C-A

134691428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812463-A-G

134691437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812471-G-A

134691447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812481-G-A

134691515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812553-C-G

134691515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812553-C-T

http://identifiers.org/hco/9/GRCh38#134691739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27812768-C-A

134691739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27812768-C-T

http://identifiers.org/hco/9/GRCh38#134691838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27812851-C-A

134691877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812881-C-T

http://identifiers.org/hco/9/GRCh38#134691893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27812894-C-A

134691893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812894-C-G

134691896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812897-G-A

134691908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812909-G-A

134691908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812909-G-T

134691969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812960-C-G

134691969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27812960-C-T

134697105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27815751-G-A

134697145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27815796-A-G

http://identifiers.org/hco/9/GRCh38#134697234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27815873-A-C

134697578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816167-C-T

134697686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816218-T-G

134697713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816240-C-T

http://identifiers.org/hco/9/GRCh38#134697740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27816244-C-A

134697804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816279-T-C

134698365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816680-T-C

134698471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816776-T-C

134698508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27816803-G-A

134699188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817414-G-A

134699188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817414-G-C

134699340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817556-T-C

134699413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817628-A-T

134699496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817669-T-A

134699496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817669-T-C

134699496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817669-T-G

134699527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817699-G-A

134699527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817699-G-T

134699764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817933-G-A

134699804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817966-G-A

134699804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27817966-G-T

134699925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27818070-G-A

http://identifiers.org/hco/9/GRCh38#134699955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27818100-C-A

134699955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27818100-C-T

134700009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27818154-G-A

134700009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27818154-G-T

http://identifiers.org/hco/9/GRCh38#134700090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27818235-C-A

134700090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27818235-C-T

http://identifiers.org/hco/9/GRCh38#134700093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27818238-C-A

134700093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27818238-C-T

134700159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818286-G-T

http://identifiers.org/hco/9/GRCh38#134700204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27818320-C-A

134700204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818320-C-T

134700217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818334-G-A

134700217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818334-G-T

134700226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818343-G-A

134700226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818343-G-T

134700304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818413-G-C

134700543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818628-G-A

134700620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818765-C-T

134700654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818795-G-A

134700654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27818795-G-C

134701126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819341-G-A

134701126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819341-G-C

134701147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819362-T-C

134701291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27819511-C-T

134701501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819700-T-C

134701520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819717-G-A

134701520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819717-G-T

134701524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819721-A-T

134701682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819862-T-C

134701791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819961-G-T

134701793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27819963-T-C

134701901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820144-C-G

134701996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820232-C-T

134702029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820251-G-A

134702147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820328-G-A

134702254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820409-T-C

134702256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820411-T-C

134702403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820559-T-C

134702514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820685-C-G

134702514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820685-C-T

134702524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820695-C-T

134702878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27820758-G-A

134702946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820803-G-A

134702994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820846-C-T

134703083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27820935-C-G

134703087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27820938-T-C

134703116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27820951-T-A

134703305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27821107-C-T

134703331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27821131-G-A

134703371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27821170-G-A

134704481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27821997-G-A

134704861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27822363-T-C

134704912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27822409-T-C

134704966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27822471-C-T

134705051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27822534-A-T

134705588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823112-G-C

http://identifiers.org/hco/9/GRCh38#134705610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27823134-A-C

http://identifiers.org/hco/9/GRCh38#134705884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27823339-C-A

134705884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823339-C-T

134705886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823365-G-A

134705886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823365-G-T

134705996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823458-C-G

134706025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823478-G-A

134706031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823484-C-T

http://identifiers.org/hco/9/GRCh38#134706350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27823733-C-A

134706350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823733-C-T

134706483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823860-C-T

134706620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27823996-A-G

134706624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27824000-C-G

134706736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27824044-C-T

134706794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27824068-C-T

134706887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27824145-C-T

134707026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27824233-C-T

134707146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27824352-C-G

http://identifiers.org/hco/9/GRCh38#134707157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27824363-C-A

134708375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27825374-G-A

134708375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27825374-G-T

134709666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27826840-G-C

134709762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27826927-C-G

134709835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27827019-G-A

134709835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27827019-G-T

134709968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27827140-C-T

134709978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27827150-G-C

134714052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828402-C-T

134714229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828551-C-G

134714236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828558-C-T

134714373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828649-G-A

134714430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828703-G-A

http://identifiers.org/hco/9/GRCh38#134714484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27828736-C-A

134714484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828736-C-G

134714484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828736-C-T

134714518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828761-A-G

134714518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828761-A-T

134714554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828789-T-A

http://identifiers.org/hco/9/GRCh38#134714564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27828799-A-C

134714564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828799-A-G

134714570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828805-A-G

134714575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828810-G-T

134714595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828830-T-C

http://identifiers.org/hco/9/GRCh38#134714700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27828920-A-C

134714700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828920-A-G

134714714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27828934-T-C

134714811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829034-G-A

134714811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829034-G-C

134717009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829235-G-C

http://identifiers.org/hco/9/GRCh38#134717072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27829301-C-A

134717072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829301-C-T

134717253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829447-C-T

134717517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829716-C-T

134717549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829756-G-A

134717558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829774-A-G

134717565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829782-G-A

134717565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829782-G-T

134717683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829907-T-C

134717711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27829934-C-T

134718536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27830651-G-A

134718931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27830948-G-A

134719233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27831241-A-G

134721904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27833566-T-C

134721926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27833588-T-C

134722284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27833721-T-C

134722524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27833905-G-A

134722730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27834118-T-C

134722946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27834320-G-A

134722946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27834320-G-C

134722995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27834390-C-T

134723001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27834396-T-C

134724151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27836845-G-A

134724154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27836848-C-G

134724154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27836848-C-T

134724306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27836993-C-T

134724430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837092-G-A

134724451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837117-T-C

134724599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837262-C-G

134724694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837309-G-A

134724694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837309-G-T

134724751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837364-A-G

134724834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837434-C-T

134725135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27837714-G-A

134726763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839147-T-G

134726774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839158-G-A

134726774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839158-G-T

134726796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839177-A-G

134726850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839231-A-G

134727100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839473-C-G

http://identifiers.org/hco/9/GRCh38#134727154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27839525-C-A

134727154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839525-C-G

134727188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839559-G-A

134727188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839559-G-T

134727195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839566-G-A

134727195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839566-G-T

134727201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839572-G-T

134727202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839573-T-C

134727217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839595-T-G

134727222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839600-G-A

134727232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839605-A-G

134727261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27839634-T-A

134727261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27839634-T-C

134727261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27839634-T-G

134727286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27839659-C-G

134727286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27839659-C-T

134727295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27839668-G-A

134727295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27839668-G-T

134727313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27839686-T-C

134727415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839788-G-A

134727415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839788-G-T

134727505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839871-G-A

134727505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839871-G-T

134727536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27839904-A-T

134727707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840096-T-C

134728313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840368-G-T

134728328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840380-G-A

134728629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840599-G-A

134728629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840599-G-T

134728648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840618-C-T

134728655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840625-G-A

134728655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840625-G-T

134728740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27840703-T-C

134728762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27840725-C-G

134728774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27840737-G-A

134728847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840814-C-G

134728847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840814-C-T

134728848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840815-G-A

134728848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840815-G-C

134728848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27840815-G-T

134730202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841267-C-T

134730215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841278-G-A

134730294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27841357-G-A

134730331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27841394-C-T

134730498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841561-G-T

134730524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841593-G-A

134730524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841593-G-T

134730553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841629-C-T

http://identifiers.org/hco/9/GRCh38#134730554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27841630-C-A

134730554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841630-C-G

134730554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841630-C-T

134730619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841677-T-A

134730619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27841677-T-C

134731292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27842079-G-T

http://identifiers.org/hco/9/GRCh38#134731301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27842084-C-A

134731382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27842157-T-C

134731382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27842157-T-G

134731537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27842320-G-T

134731920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27842854-T-C

http://identifiers.org/hco/9/GRCh38#134731931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27842865-C-A

134731931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27842865-C-T

134731955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27842890-G-T

134732051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27842973-C-T

134732155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843183-G-A

http://identifiers.org/hco/9/GRCh38#134732236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27843258-C-A

134732262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843279-T-A

134732266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843283-G-A

134732266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843283-G-C

134732268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843285-G-A

134732282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843297-A-G

134732356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843376-G-A

134732356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843376-G-T

134732426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843440-A-G

134732426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843440-A-T

http://identifiers.org/hco/9/GRCh38#134732444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27843451-C-A

134732444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843451-C-G

134732444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843451-C-T

134732460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843467-T-C

134732468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843468-G-C

134732468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843468-G-T

http://identifiers.org/hco/9/GRCh38#134732517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27843497-C-A

134732517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843497-C-G

134732517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843497-C-T

134732545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843523-G-A

134732545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843523-G-T

134732611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27843579-T-C

134732699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27843659-G-T

http://identifiers.org/hco/9/GRCh38#134732711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27843671-A-C

134732711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27843671-A-G

134732806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27843747-G-A

134732806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27843747-G-T

134732926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27843836-C-T

134733151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844086-C-T

134733207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844121-A-G

134733633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844486-G-A

134733633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844486-G-C

134733725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844549-G-A

134733932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844742-C-T

134733933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844743-G-A

134733933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844743-G-C

134734149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844918-G-A

134734180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844949-G-T

134734194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27844963-G-C

134734390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27845115-T-C

http://identifiers.org/hco/9/GRCh38#134734495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27845220-C-A

134734625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27845384-G-A

134735559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27846771-G-C

134735723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27846925-G-T

134735774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27846977-C-T

134735798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27846990-C-T

134735809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27847001-C-T

134735836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27847027-T-G

134735869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27847060-C-T

134738194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848012-C-G

134738194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848012-C-T

134738235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848054-G-T

134738323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848119-C-T

134738395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848161-A-G

134738485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27848245-C-G

134738485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27848245-C-T

134738518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848278-G-A

134738569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848336-G-C

134738597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848353-A-T

http://identifiers.org/hco/9/GRCh38#134738626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27848381-C-A

134738626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848381-C-T

134738633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848388-C-T

134738637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848389-G-A

134738638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848390-G-A

http://identifiers.org/hco/9/GRCh38#134738868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27848645-C-A

134738868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848645-C-T

http://identifiers.org/hco/9/GRCh38#134738881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27848658-C-A

134738881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848658-C-T

http://identifiers.org/hco/9/GRCh38#134738951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27848735-C-A

134738951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848735-C-G

134738951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27848735-C-T

134750087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27849995-C-T

134750109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850024-A-G

134750266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850158-C-T

134750281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850175-T-C

134750299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850192-G-C

134750320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850211-T-C

134750417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850290-A-G

134750473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850329-C-T

134750500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850358-T-C

134750624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27850481-C-T

134750637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27850492-G-A

134750795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27852079-G-A

134750798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27852082-T-C

134750810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27852094-C-T

134750831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27852115-C-G

134750831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27852115-C-T

134750984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852243-G-A

134750984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852243-G-T

134750991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852250-T-G

134751133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852330-C-T

134751226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852390-G-A

134751499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852478-C-T

134751520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852499-G-T

134751674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852645-G-A

134751726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852675-T-G

134751738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852687-A-G

134751741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852690-C-T

http://identifiers.org/hco/9/GRCh38#134751811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27852761-C-A

134751824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852774-A-G

134751869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27852813-C-T

134752229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27853760-G-A

134752309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27853828-C-T

134752356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27853876-C-T

134752358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27853878-C-T

http://identifiers.org/hco/9/GRCh38#134752387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27853905-A-C

134752552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854043-G-T

134752565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854056-A-G

134752570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854061-G-A

http://identifiers.org/hco/9/GRCh38#134752575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27854066-A-C

134752575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854066-A-G

http://identifiers.org/hco/9/GRCh38#134752757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27854186-C-A

134752757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854186-C-G

134752854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854267-G-C

134752991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854365-T-C

134753032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854409-G-A

134753072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854457-C-T

134753104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854488-C-T

134753185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854604-G-A

134753281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27854715-G-A

134753549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855013-C-T

134753653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855116-C-T

134753690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855152-C-G

134753707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855162-G-A

134753707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855162-G-T

http://identifiers.org/hco/9/GRCh38#134753762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855195-C-A

134753762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855195-C-T

http://identifiers.org/hco/9/GRCh38#134753767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855200-C-A

134753767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855200-C-G

134753767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855200-C-T

http://identifiers.org/hco/9/GRCh38#134753832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855249-C-A

http://identifiers.org/hco/9/GRCh38#134753982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855380-C-A

134753982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855380-C-T

134754008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855407-A-G

http://identifiers.org/hco/9/GRCh38#134754142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855487-C-A

134754142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855487-C-G

134754142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855487-C-T

134754143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855488-G-A

134754143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855488-G-T

134754172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855517-G-A

134754172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855517-G-T

http://identifiers.org/hco/9/GRCh38#134754192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855537-A-C

http://identifiers.org/hco/9/GRCh38#134754215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27855552-C-A

134754215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855552-C-T

134754299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27855635-T-C

134754342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855683-G-A

134754697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855953-A-G

134754734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27855982-C-T

134756030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856275-G-A

134756171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856393-C-T

134756192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856421-C-T

134756267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856518-G-A

134756285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856534-G-A

134756403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856648-C-T

134756466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856704-C-T

134756467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856705-A-G

134756479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856712-T-A

134756552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856745-C-T

134756616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856805-T-G

134756753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856930-C-G

134756753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27856930-C-T

134756809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27856986-T-A

134756809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27856986-T-C

134756809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27856986-T-G

134756825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27857002-C-T

134756870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857039-G-A

134756870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857039-G-T

http://identifiers.org/hco/9/GRCh38#134756889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27857058-C-A

134756889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857058-C-T

134756909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857077-G-A

134756909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857077-G-T

134756929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857110-G-A

134756929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857110-G-C

134756929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857110-G-T

134756931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857112-G-A

134756932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857113-G-A

134756932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857113-G-T

http://identifiers.org/hco/9/GRCh38#134756940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27857121-A-C

134756940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857121-A-G

134756984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857156-A-G

134757117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857278-G-A

134757223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857394-G-A

134757258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857415-C-T

134757261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857418-G-T

134757295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857439-C-T

134757635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857644-T-C

134757820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857814-G-A

134757847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27857836-G-A

134758070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858011-G-A

http://identifiers.org/hco/9/GRCh38#134758103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27858048-C-A

134758103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858048-C-T

134758177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858096-A-T

134758190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858105-G-A

134758190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858105-G-C

134758190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858105-G-T

134758498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858322-A-G

134759237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858744-A-T

http://identifiers.org/hco/9/GRCh38#134759439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27858930-A-C

134759439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858930-A-G

http://identifiers.org/hco/9/GRCh38#134759447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27858938-C-A

134759447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858938-C-G

134759447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858938-C-T

134759484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858979-C-T

134759497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27858992-A-G

134759505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859002-G-A

134759505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859002-G-C

134759619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859122-T-A

134759619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859122-T-C

134759619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859122-T-G

134759664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859169-G-A

134759664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859169-G-T

134761445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859308-A-G

134761536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859407-G-A

134761769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859616-C-T

134761771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859618-C-T

134761772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859619-G-T

134761775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859622-A-G

134761824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859661-G-A

134761824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859661-G-T

134761848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859675-A-G

134761877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859706-T-C

134761877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859706-T-G

134761960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27859792-G-A

134762033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859833-T-C

134762069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859865-G-A

http://identifiers.org/hco/9/GRCh38#134762110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27859904-C-A

134762146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859931-A-G

134762146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859931-A-T

134762150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27859935-C-T

134762401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860169-G-A

134762401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860169-G-T

134762464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860210-G-A

134762521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860262-A-G

134762521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860262-A-T

134762540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860302-T-C

134762849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860531-T-G

134762875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860562-G-T

134762954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860649-A-T

134762976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860671-G-A

134762976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860671-G-C

134763012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860699-G-A

134763012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860699-G-C

134763159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860800-C-T

134763249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860886-C-T

134763330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27860957-G-A

134763560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861165-T-G

134763698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27861464-C-T

134763825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861559-A-G

134763860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861590-G-T

134763868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861598-G-A

134763868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861598-G-T

http://identifiers.org/hco/9/GRCh38#134763871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27861601-C-A

134763871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861601-C-T

134763957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861683-G-A

134764409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861949-G-T

134764443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861973-C-G

134764443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27861973-C-T

134764814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862325-G-A

134764898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862409-A-G

134765081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862614-C-T

134765102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862635-G-A

134765289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862797-G-A

134765306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862814-G-A

134765341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862839-T-C

134765449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27862933-G-C

http://identifiers.org/hco/9/GRCh38#134765536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863020-C-A

134765567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863043-T-C

134765567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863043-T-G

134765587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863062-T-C

http://identifiers.org/hco/9/GRCh38#134765594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863069-A-C

134765595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863070-G-T

134765665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863144-C-T

http://identifiers.org/hco/9/GRCh38#134765752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863231-C-A

134765752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863231-C-G

134765752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863231-C-T

http://identifiers.org/hco/9/GRCh38#134765756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863235-C-A

134765756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863235-C-G

134765813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863299-G-A

134765813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863299-G-T

134765820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863306-G-A

134765820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863306-G-T

134765824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863310-G-A

134765824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863310-G-T

http://identifiers.org/hco/9/GRCh38#134765825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863311-C-A

134765825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863311-C-T

http://identifiers.org/hco/9/GRCh38#134765839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863325-C-A

134765839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863325-C-T

134765856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863339-T-A

134765856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863339-T-C

134766170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863652-A-G

134766412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863851-T-C

134766412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863851-T-G

134766414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863853-G-A

134766414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863853-G-C

134766414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863853-G-T

http://identifiers.org/hco/9/GRCh38#134766419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863858-C-A

134766419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863858-C-T

134766520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863946-G-A

134766526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863952-C-T

http://identifiers.org/hco/9/GRCh38#134766535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27863960-C-A

134766535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27863960-C-T

134766817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864250-A-G

134766904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864368-G-T

http://identifiers.org/hco/9/GRCh38#134766918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27864380-C-A

134766918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864380-C-T

http://identifiers.org/hco/9/GRCh38#134766919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27864381-C-A

134766919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864381-C-T

http://identifiers.org/hco/9/GRCh38#134766941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27864400-C-A

134766952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864409-T-G

134766953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864410-A-G

134766977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864434-G-A

134766984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864441-C-T

134767014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27864470-G-A

134767014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27864470-G-T

134767088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864544-C-G

134767088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864544-C-T

134767230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864636-G-C

134767254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864659-G-A

134767254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864659-G-T

134767291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864690-G-T

134767363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864758-G-T

http://identifiers.org/hco/9/GRCh38#134767407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27864802-C-A

134767407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27864802-C-T

134767737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865037-G-A

134767908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865185-C-T

134767952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865222-G-C

http://identifiers.org/hco/9/GRCh38#134768141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27865364-A-C

http://identifiers.org/hco/9/GRCh38#134768161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27865384-A-C

134768161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865384-A-G

134768328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865469-G-T

http://identifiers.org/hco/9/GRCh38#134768368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27865510-C-A

134768368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865510-C-T

134768601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865716-G-T

134768642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865751-C-T

134768682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865792-G-A

134768682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865792-G-T

134768692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865802-A-T

134768729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27865834-G-A

134768907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27866018-G-C

134768970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27866091-G-A

134768989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27866109-G-C

134769410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27867105-T-C

134770538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27868608-A-G

134771006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869254-C-T

134771253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869481-C-T

134771448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869652-G-A

134771448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869652-G-C

134771714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869844-G-A

134771732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869861-C-T

134771773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869901-C-G

134771807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869934-C-T

134771887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27869990-T-C

134772272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27870288-C-G

134772360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27870377-C-T

134772736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27870429-G-T

134774406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27870652-C-T

134774543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27870784-A-G

http://identifiers.org/hco/9/GRCh38#134774760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27870966-C-A

134774760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27870966-C-T

http://identifiers.org/hco/9/GRCh38#134774820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27871012-C-A

134774820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871012-C-T

134774954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871143-G-C

134774960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871151-G-A

http://identifiers.org/hco/9/GRCh38#134774970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27871161-C-A

134774970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871161-C-T

http://identifiers.org/hco/9/GRCh38#134775047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27871233-C-A

134775049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871235-G-T

134775143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871330-C-T

134775319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27871475-T-C

134775976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27872084-G-A

134776078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27872175-C-T

134776156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27872219-G-A

134776241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27872302-T-G

134776300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27872360-G-A

134776422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27872480-A-G

134776514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27872566-A-T

134776852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27872838-A-G

134776852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27872838-A-T

134776860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27872846-G-A

134778452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27873548-C-T

134778542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27873637-T-A

134778651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27873760-C-T

134778663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27873770-C-T

134778759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27873848-A-G

http://identifiers.org/hco/9/GRCh38#134778792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#27873868-C-A

134778792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27873868-C-G

http://identifiers.org/hco/9/GRCh38#134778850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#27873923-C-A

134778972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27874009-A-G

http://identifiers.org/hco/9/GRCh38#134779134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27874144-C-A

134779208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27874204-C-T

134779325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27874336-G-A

134779408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27874414-T-G

134779663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27874655-G-A

134779756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27874735-G-A

134779965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27874955-G-A

134779973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27874963-G-T

http://identifiers.org/hco/9/GRCh38#134780153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27875116-C-A

134780153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27875116-C-G

134780153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27875116-C-T

134780176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875132-C-T

134780177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875133-C-G

http://identifiers.org/hco/9/GRCh38#134780286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27875195-A-C

134780286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875195-A-G

134780286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875195-A-T

134780345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875233-C-T

134780520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875394-G-A

134780581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875459-A-G

134780609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875493-G-A

134780609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875493-G-C

134780669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875551-T-A

134780695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875577-C-G

134781123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27875914-C-G

134781266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876033-A-T

134781318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876078-C-T

134781319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876079-G-A

134781319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876079-G-T

134781391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876167-G-A

134781418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876197-G-A

134781428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876208-C-T

134781472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876260-G-A

134781505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876304-T-G

134781581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876390-C-G

http://identifiers.org/hco/9/GRCh38#134781706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27876508-C-A

134782659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27876725-A-G

134782787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876855-T-A

134782787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876855-T-C

134782787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876855-T-G

134782840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27876907-T-C

134782988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27877070-G-A

134783077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27877128-A-G

134783168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27877213-C-T

134783463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27877581-G-A

134783628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27877730-G-A

http://identifiers.org/hco/9/GRCh38#134783942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27878018-C-A

134784083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27878241-G-A

134784169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27878356-A-T

134784297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27878474-C-T

134784518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27878653-C-T

134784723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27878938-G-C

134784791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27878964-G-A

134784851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879024-G-A

134784851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879024-G-C

134784854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879027-A-G

134784854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879027-A-T

134784873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879038-G-A

134784873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879038-G-C

134784873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879038-G-T

134784887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879054-G-A

http://identifiers.org/hco/9/GRCh38#134784909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27879065-C-A

134784909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879065-C-T

134784994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27879156-G-T

134785136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879294-A-T

134785169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879317-C-G

134785322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879465-A-G

134785509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879618-A-G

134785520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879628-A-T

134785558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879659-C-T

134785643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879742-T-G

134785651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879750-C-T

134785662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879761-A-G

134785678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879776-G-T

134785881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879947-G-T

http://identifiers.org/hco/9/GRCh38#134785922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27879974-C-A

134785940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879992-G-A

134785940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879992-G-T

134785946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27879998-G-T

http://identifiers.org/hco/9/GRCh38#134786236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27880153-A-C

134786372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27880242-C-T

http://identifiers.org/hco/9/GRCh38#134786475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27880348-C-A

134786786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27880605-G-T

134786992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27880765-G-A

134787373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881063-C-T

134787540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881325-C-T

134787589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881426-C-T

134787590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881427-A-G

134787593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881430-G-T

134787735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881539-G-A

http://identifiers.org/hco/9/GRCh38#134787942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27881740-A-C

134787949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881747-A-G

134789008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881848-A-T

134789017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881857-T-C

134789017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881857-T-G

134789020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881860-G-A

134789020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881860-G-T

134789049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881894-G-A

134789049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881894-G-C

134789049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881894-G-T

http://identifiers.org/hco/9/GRCh38#134789090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27881936-C-A

134789090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27881936-C-T

http://identifiers.org/hco/9/GRCh38#134789251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27882075-C-A

134789251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882075-C-T

134789286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882108-G-A

134789286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882108-G-T

134789337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882159-G-A

134789337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882159-G-T

134789352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882173-A-G

134789358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882179-A-G

134789532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27882307-G-A

134791970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27883681-C-T

134792033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27883729-C-G

134792242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27883886-C-T

134792956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884077-T-A

134792956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884077-T-C

http://identifiers.org/hco/9/GRCh38#134792959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27884080-C-A

134792959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884080-C-G

134792959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884080-C-T

134792995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884115-C-T

134793010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884130-C-T

134793113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884235-G-A

134793453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884506-A-G

134793507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884559-G-A

134793527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884577-G-T

134793551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884612-C-T

134793613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884674-A-G

134793632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884689-G-A

http://identifiers.org/hco/9/GRCh38#134793678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27884713-C-A

134793778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884806-G-A

134793778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27884806-G-C

134794401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885119-G-T

134794551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885286-C-T

134794726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885454-A-G

134794941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885573-G-A

134794941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885573-G-C

http://identifiers.org/hco/9/GRCh38#134794985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27885595-C-A

http://identifiers.org/hco/9/GRCh38#134794992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27885602-C-A

134794992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885602-C-T

134795015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885652-G-A

134795015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885652-G-T

134795267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27885878-G-A

134795267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27885878-G-C

134795306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27885917-T-G

134795329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885938-C-T

134795331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27885940-C-T

http://identifiers.org/hco/9/GRCh38#134795465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27886028-C-A

134795465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886028-C-G

134795522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886076-T-A

134795661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886213-G-A

134795661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886213-G-T

134795680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886232-G-A

134795713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886258-G-T

134796029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886643-A-G

134796403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27886910-C-T

134796463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886977-G-A

134796463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27886977-G-C

http://identifiers.org/hco/9/GRCh38#134796489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27886998-C-A

134796540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887045-G-C

134796540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887045-G-T

134796544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887049-T-C

134796572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887075-C-T

134796727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887483-G-A

134796727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887483-G-T

134796731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887487-A-G

134796765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887494-G-A

134796780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887508-G-A

134796791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887519-G-A

134796797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887525-G-A

134796797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887525-G-T

http://identifiers.org/hco/9/GRCh38#134796832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27887559-C-A

134796832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887559-C-G

134796833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27887560-T-C

http://identifiers.org/hco/9/GRCh38#134798365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27888692-C-A

134798365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888692-C-T

http://identifiers.org/hco/9/GRCh38#134798455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27888785-C-A

134798455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27888785-C-T

134798527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888853-G-A

134798527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888853-G-T

134798565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888902-T-A

134798565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888902-T-C

134798565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888902-T-G

134798566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888903-G-A

134798566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888903-G-T

http://identifiers.org/hco/9/GRCh38#134798608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27888945-C-A

134798617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888954-G-A

134798638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888975-G-A

http://identifiers.org/hco/9/GRCh38#134798670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27888982-C-A

134798670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888982-C-T

http://identifiers.org/hco/9/GRCh38#134798671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27888983-C-A

134798671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888983-C-T

134798672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27888984-G-A

134798774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889080-C-G

134798852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889142-T-C

134798902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889184-C-T

134798930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889211-C-T

134798955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889243-G-T

134799335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889590-A-G

134799450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27889689-A-G

134801911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27891540-A-G

134801911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27891540-A-T

134802040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27891668-A-T

134802320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27891919-C-G

134802320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27891919-C-T

134802362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27891968-C-T

134802523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892125-T-A

134802523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892125-T-G

134802536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892138-G-C

http://identifiers.org/hco/9/GRCh38#134802659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27892228-A-C

134802672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892241-G-A

134802738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892296-G-T

http://identifiers.org/hco/9/GRCh38#134802774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27892332-C-A

134802774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892332-C-T

134802783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892341-G-T

http://identifiers.org/hco/9/GRCh38#134802799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27892398-A-C

134802799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892398-A-G

134802804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892403-G-A

134802804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892403-G-T

http://identifiers.org/hco/9/GRCh38#134802850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27892448-C-A

134802878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892485-T-C

134802878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892485-T-G

134803016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892623-G-A

134803016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892623-G-C

134803204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27892772-G-T

134804308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893262-G-A

134804357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893309-G-A

134804393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893333-C-T

134804587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893513-C-T

134804592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893518-A-T

134804599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893530-G-C

134804673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893634-G-A

134804749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893708-C-G

134804825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893743-G-A

134804825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893743-G-C

http://identifiers.org/hco/9/GRCh38#134804846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27893756-C-A

134804850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893760-G-A

134804850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893760-G-T

134804871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893778-G-C

134804871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893778-G-T

134804886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893793-G-A

134804886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893793-G-T

134804922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893819-G-A

134804922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893819-G-T

134804942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893839-T-C

134804965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893862-C-T

134805061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27893959-A-G

134805067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27893965-G-A

134805225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894118-G-A

134805225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894118-G-T

134805297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894162-T-C

134805317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894182-G-A

134805317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894182-G-T

134805360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894196-G-C

134805604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894409-G-A

134805892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894875-C-T

134805908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894895-G-A

134805912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894901-G-T

134805981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894968-G-A

134805981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27894968-G-T

http://identifiers.org/hco/9/GRCh38#134806053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27895061-C-A

134806053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895061-C-T

134806067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895077-T-C

134806067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895077-T-G

http://identifiers.org/hco/9/GRCh38#134806096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27895106-C-A

134806096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895106-C-T

134806114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895124-A-G

http://identifiers.org/hco/9/GRCh38#134806127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27895130-C-A

134806127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895130-C-G

134806127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895130-C-T

134806137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895139-A-G

http://identifiers.org/hco/9/GRCh38#134806143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27895145-C-A

134806143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895145-C-T

134806388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895365-A-T

134806390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895367-G-T

134806393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895370-T-C

134806393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895370-T-G

134806394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895371-A-T

134806395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895372-T-C

134806403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895380-G-C

134806403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895380-G-T

134806597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895483-C-T

134806696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895560-C-T

134806761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27895628-G-T

http://identifiers.org/hco/9/GRCh38#134807805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27896187-A-C

134807835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896215-A-G

http://identifiers.org/hco/9/GRCh38#134807906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27896281-C-A

134807906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896281-C-G

134807968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896341-A-G

134808247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896536-G-A

134808471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896756-G-T

134808482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896767-C-T

134808515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896800-C-T

http://identifiers.org/hco/9/GRCh38#134808556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27896844-C-A

http://identifiers.org/hco/9/GRCh38#134808608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27896908-A-C

134808663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27896972-C-T

134808896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27897399-T-A

134808896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27897399-T-C

134808896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27897399-T-G

http://identifiers.org/hco/9/GRCh38#134808901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27897404-A-C

134808901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27897404-A-G

http://identifiers.org/hco/9/GRCh38#134808948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27897462-C-A

134808963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897506-T-G

134808966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897509-G-A

134808966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897509-G-T

134808989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897571-G-A

134809021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897600-G-A

134809021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897600-G-T

134809038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897616-G-A

134809038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897616-G-T

http://identifiers.org/hco/9/GRCh38#134809055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27897631-C-A

134809056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897632-T-G

134809061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897637-G-A

134809061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897637-G-T

134809130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897708-G-A

134809133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897711-T-G

134809134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897712-G-A

134809134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897712-G-T

134809162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897740-G-T

http://identifiers.org/hco/9/GRCh38#134809167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27897744-C-A

134809167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897744-C-G

134809167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27897744-C-T

134809327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897893-G-A

134809327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897893-G-T

134809370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897929-A-G

134809400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897955-G-T

http://identifiers.org/hco/9/GRCh38#134809401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27897956-C-A

134809401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897956-C-G

134809401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897956-C-T

134809416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27897971-C-T

134809498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27898059-C-T

134809615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27898178-G-A

134810027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27898567-A-G

134810214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27899029-T-C

134810236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27899101-C-T

134810465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899315-G-A

134810465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899315-G-T

134810479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899329-G-A

134810489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899333-C-G

134810536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899366-G-T

134810759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899508-G-A

134810877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899580-C-T

134810979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899683-A-G

134811162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27899856-C-T

134811293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900003-T-C

134811298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900008-G-A

134811298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900008-G-C

134811298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900008-G-T

134811447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900138-T-A

134811560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27900250-C-T

134811629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900313-T-C

134811876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27900594-C-T

134811908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27900622-A-G

http://identifiers.org/hco/9/GRCh38#134812044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#27900721-C-A

134812067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: 27900741-G-A

http://identifiers.org/hco/9/GRCh38#134812133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27900815-A-C

134812133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27900815-A-G

http://identifiers.org/hco/9/GRCh38#134812177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#27900860-C-A

134812367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901028-G-A

134812367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901028-G-T

134812389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901050-G-A

134812389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901050-G-T

134812408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901066-A-G

134812408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901066-A-T

134812420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901078-C-G

134812420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901078-C-T

134812703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27901352-G-A

134812703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27901352-G-T

134812718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901367-G-A

134812718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901367-G-T

134812728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901377-G-A

134812728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901377-G-C

134812734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901383-G-A

http://identifiers.org/hco/9/GRCh38#134812746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27901395-C-A

134812746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901395-C-G

134812746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901395-C-T

134812747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901396-G-A

134812747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901396-G-C

134812747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901396-G-T

134812755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901404-G-A

134812755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901404-G-C

134812755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901404-G-T

http://identifiers.org/hco/9/GRCh38#134812774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27901422-C-A

134812774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901422-C-G

134812779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901427-T-A

134812808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901454-G-A

134812808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901454-G-T

134812814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901460-A-G

134812814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901460-A-T

http://identifiers.org/hco/9/GRCh38#134812815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27901461-C-A

134812815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901461-C-T

134812820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901466-T-A

134812820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901466-T-C

134812820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901466-T-G

http://identifiers.org/hco/9/GRCh38#134812837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27901491-C-A

134812837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901491-C-T

http://identifiers.org/hco/9/GRCh38#134812863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27901517-C-A

134812863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901517-C-T

134812892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901545-C-T

134812911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901563-T-C

134812983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901628-G-A

134812986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901631-T-A

134813138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901779-C-T

134813188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27901832-C-G

http://identifiers.org/hco/9/GRCh38#134813758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27902441-C-A

134813793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902483-G-A

134813796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902486-C-T

http://identifiers.org/hco/9/GRCh38#134813919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27902631-A-C

134813919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902631-A-G

http://identifiers.org/hco/9/GRCh38#134813966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27902670-A-C

134813966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902670-A-G

134813988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27902692-G-A

134813988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: missense variant
orthologous variants: 27902692-G-T

http://identifiers.org/hco/9/GRCh38#134814046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27902747-C-A

134814046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902747-C-T

134814049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902750-G-A

134814049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902750-G-T

134814149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902849-G-A

134814152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27902852-G-A

134814303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903042-C-T

134814315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903056-T-A

134814565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903224-C-T

134814610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903265-C-G

134814662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903314-G-A

134814662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903314-G-C

134814662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903314-G-T

134814673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903325-G-A

134814673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903325-G-T

134814761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903435-G-T

134814968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903633-T-C

134814970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903635-T-A

134814970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903635-T-C

134814985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903662-G-A

134814985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903662-G-T

http://identifiers.org/hco/9/GRCh38#134814988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27903665-C-A

134814989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903666-T-C

134814989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903666-T-G

134815047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903725-A-G

134815117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903796-C-T

134815202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903849-G-A

134815248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903868-C-T

134815315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27903910-G-A

134815484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904051-G-T

http://identifiers.org/hco/9/GRCh38#134815514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27904071-C-A

134815514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904071-C-T

134815638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904181-T-A

134815725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904260-G-T

134815846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904304-G-T

134815854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904312-G-A

134816024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27904468-G-A

134816591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905432-G-A

134816591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905432-G-C

134816620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905461-G-A

134816620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905461-G-C

http://identifiers.org/hco/9/GRCh38#134816896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27905731-C-A

134816896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905731-C-T

134816937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905759-G-A

134816937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905759-G-T

134816945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905768-A-G

134816945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905768-A-T

134816963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905786-T-G

http://identifiers.org/hco/9/GRCh38#134816998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27905838-C-A

134816998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905838-C-T

134817001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905841-A-G

134817034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27905874-C-G

134817034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27905874-C-T

134817160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905958-G-A

http://identifiers.org/hco/9/GRCh38#134817163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27905961-C-A

134817163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905961-C-T

134817179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905977-G-A

134817179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905977-G-T

134817194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905990-G-A

134817194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27905990-G-T

134817228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906012-G-A

134817228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906012-G-C

134817228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906012-G-T

134817291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906089-G-A

134817291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906089-G-C

134817291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906089-G-T

134817442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906223-G-A

134817593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906336-G-A

http://identifiers.org/hco/9/GRCh38#134817631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27906377-C-A

134817631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906377-C-G

134817631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906377-C-T

http://identifiers.org/hco/9/GRCh38#134817653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27906399-C-A

134817653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906399-C-T

134817659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906405-A-G

134817660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906406-G-A

134817660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906406-G-T

http://identifiers.org/hco/9/GRCh38#134817698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27906425-C-A

134817698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906425-C-G

134817698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906425-C-T

134818252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906775-G-C

134818252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906775-G-T

http://identifiers.org/hco/9/GRCh38#134818280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27906803-C-A

134818280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906803-C-T

134818307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906832-T-A

134818308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27906833-G-T

http://identifiers.org/hco/9/GRCh38#134818432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27906937-A-C

134818535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907020-C-T

http://identifiers.org/hco/9/GRCh38#134818541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27907026-A-C

134818541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907026-A-G

134818541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907026-A-T

134818543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907028-G-T

134818597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907067-G-A

134818597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907067-G-T

134818634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907091-T-C

134818636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907092-T-C

134818637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907093-G-T

134818733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: synonymous variant
orthologous variants: 27907184-G-A

134818770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27907221-A-G

134818812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907269-G-A

134818821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907278-C-G

134818821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907278-C-T

134818909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 27907354-A-G

134818933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907371-G-C

134818933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907371-G-T

134818961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907399-C-T

134818967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907405-T-C

134818991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907429-C-G

134818991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907429-C-T

134819075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907515-C-T

134819077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907517-G-A

134819077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907517-G-T

134819160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907616-G-A

134819160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907616-G-T

134819193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron variant
orthologous variants: 27907646-G-A

134819562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27907847-T-C

134819642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27907881-A-G

134819707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27907947-A-G

134819994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908333-G-A

134819994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908333-G-T

134819997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908336-G-A

134819997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908336-G-T

134820045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908382-A-G

134820048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908385-G-A

134820049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908386-G-A

134820056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908393-G-A

134820059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908397-G-A

134820073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908411-G-A

134820073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908411-G-T

134820076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908414-G-A

134820076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908414-G-C

http://identifiers.org/hco/9/GRCh38#134820089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27908427-C-A

134820089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27908427-C-T

134820142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27908479-C-T

134820145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27908482-T-C

134820151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27908488-G-A

134820151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27908488-G-C

134820151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27908488-G-T

134820271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908576-A-T

http://identifiers.org/hco/9/GRCh38#134820316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27908611-C-A

134820316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908611-C-G

http://identifiers.org/hco/9/GRCh38#134820371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27908665-A-C

134820371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908665-A-G

134820378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908671-C-T

134820385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908678-G-A

http://identifiers.org/hco/9/GRCh38#134820601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27908876-C-A

134820601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908876-C-G

134820601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908876-C-T

134820687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908989-T-C

134820695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27908997-A-G

134820775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909041-C-T

134820875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909110-C-T

134820890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909122-G-A

134820986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909213-G-T

134820999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909226-T-C

134821020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909247-G-A

http://identifiers.org/hco/9/GRCh38#134821064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27909287-A-C

134821068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909291-T-C

134821116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909324-G-A

134821274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909394-A-G

134821277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909397-G-C

134821490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909489-G-A

134821546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909528-T-C

134821797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909653-A-T

http://identifiers.org/hco/9/GRCh38#134821891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27909720-C-A

134821899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909724-T-C

134821913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909738-G-A

http://identifiers.org/hco/9/GRCh38#134821957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27909810-C-A

134821957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909810-C-T

134821966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909815-G-A

134821966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909815-G-T

134821972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909817-G-A

134821972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909817-G-T

134822004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909854-G-A

134822004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909854-G-T

134822032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909880-G-A

134822032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909880-G-T

134822035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27909883-T-G

http://identifiers.org/hco/9/GRCh38#134822164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910025-A-C

134822164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910025-A-G

134822164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910025-A-T

134822171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910032-T-C

134822171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910032-T-G

http://identifiers.org/hco/9/GRCh38#134822179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910043-C-A

134822179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910043-C-T

http://identifiers.org/hco/9/GRCh38#134822189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910053-C-A

134822189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910053-C-G

134822189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910053-C-T

http://identifiers.org/hco/9/GRCh38#134822190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910054-A-C

134822190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910054-A-G

134822190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910054-A-T

134822207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910071-G-A

134822207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910071-G-T

134822234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910082-G-C

134822254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910102-G-A

134822254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910102-G-T

134822280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910119-G-A

134822280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910119-G-T

http://identifiers.org/hco/9/GRCh38#134822284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910123-A-C

http://identifiers.org/hco/9/GRCh38#134822290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910129-C-A

134822290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910129-C-T

134822388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910231-C-G

134822437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910281-G-A

134822530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910375-C-T

134822531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910376-G-A

134822789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910613-A-G

http://identifiers.org/hco/9/GRCh38#134822809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910639-C-A

134822809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910639-C-T

http://identifiers.org/hco/9/GRCh38#134822823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910649-C-A

134822823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910649-C-T

http://identifiers.org/hco/9/GRCh38#134822837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910661-C-A

134822837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910661-C-T

134822926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27910724-G-A

134822926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27910724-G-T

134822945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27910727-G-A

134822985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27910767-C-T

134823113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910895-A-G

http://identifiers.org/hco/9/GRCh38#134823114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910896-C-A

134823114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910896-C-T

http://identifiers.org/hco/9/GRCh38#134823117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910899-A-C

134823122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910901-A-G

http://identifiers.org/hco/9/GRCh38#134823123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910902-C-A

134823123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910902-C-T

134823126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910905-T-G

134823130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910909-A-G

134823131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910910-G-T

http://identifiers.org/hco/9/GRCh38#134823134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910913-C-A

134823134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910913-C-T

http://identifiers.org/hco/9/GRCh38#134823135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27910914-A-C

134823135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27910914-A-G

134823382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912259-G-A

134823436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27912313-T-C

http://identifiers.org/hco/9/GRCh38#134823538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27912382-A-C

134823551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912395-T-A

134823551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912395-T-C

http://identifiers.org/hco/9/GRCh38#134823556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27912400-C-A

134823556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912400-C-T

134823574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912419-G-A

134823574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912419-G-T

http://identifiers.org/hco/9/GRCh38#134823576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27912421-C-A

134823578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912423-A-G

http://identifiers.org/hco/9/GRCh38#134823613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27912447-C-A

134823613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912447-C-G

134823613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912447-C-T

134823659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912498-A-T

134823778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912628-T-A

134823803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912653-G-A

http://identifiers.org/hco/9/GRCh38#134823825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27912686-C-A

134823825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912686-C-T

134823976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912864-A-G

134823976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912864-A-T

134824000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27912897-C-T

http://identifiers.org/hco/9/GRCh38#134824552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27914570-C-A

http://identifiers.org/hco/9/GRCh38#134824553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27914571-C-A

134824553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914571-C-G

134824553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914571-C-T

134824562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914580-C-T

http://identifiers.org/hco/9/GRCh38#134824566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27914584-C-A

134824566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914584-C-T

134824572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914590-C-T

134824573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914591-C-T

134824576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914594-C-G

134824576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914594-C-T

http://identifiers.org/hco/9/GRCh38#134824597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27914614-C-A

134824597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 27914614-C-G

134824617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27914634-C-T

134824689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27914706-G-A

134824689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27914706-G-C

134824704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27914721-C-T

134824705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27914722-G-A

134824945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914886-A-G

134824945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914886-A-T

134824962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27914903-A-G

http://identifiers.org/hco/9/GRCh38#134824979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27914917-C-A

http://identifiers.org/hco/9/GRCh38#134825258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915113-C-A

134825258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915113-C-T

134825325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915174-T-C

134825361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915210-T-C

134825451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915294-T-A

http://identifiers.org/hco/9/GRCh38#134825457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915300-A-C

134825646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915467-A-G

134825717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915537-A-G

http://identifiers.org/hco/9/GRCh38#134825718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915538-C-A

134825718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915538-C-G

134825718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915538-C-T

http://identifiers.org/hco/9/GRCh38#134825719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915539-A-C

134825719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915539-A-T

134825729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915550-G-A

134825729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915550-G-T

http://identifiers.org/hco/9/GRCh38#134825757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915578-C-A

134825757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915578-C-G

134825757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915578-C-T

http://identifiers.org/hco/9/GRCh38#134825775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915588-C-A

134825775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915588-C-G

134825820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27915633-A-T

134825956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915746-G-T

134825957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915747-G-A

134825957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915747-G-C

http://identifiers.org/hco/9/GRCh38#134826015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915806-A-C

134826015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915806-A-G

134826015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915806-A-T

134826018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915809-G-A

134826018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915809-G-C

134826018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915809-G-T

134826032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915823-A-G

134826032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915823-A-T

http://identifiers.org/hco/9/GRCh38#134826039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27915830-C-A

134826054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27915845-T-G

134826325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916101-C-T

134826401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916169-G-T

134826999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916358-G-A

134827220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916513-C-T

134827244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916533-C-T

http://identifiers.org/hco/9/GRCh38#134827280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27916569-C-A

134827582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916779-A-G

134827692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27916866-G-A

134828170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27917269-T-G

134828233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27917315-C-T

134828449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27917564-C-T

http://identifiers.org/hco/9/GRCh38#134828479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27917592-C-A

134828479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27917592-C-G

134828479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27917592-C-T

134828480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27917593-G-A

http://identifiers.org/hco/9/GRCh38#134830301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27919294-C-A

134830301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27919294-C-T

http://identifiers.org/hco/9/GRCh38#134830302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27919295-A-C

134830302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27919295-A-G

134830326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27919319-T-A

134830326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27919319-T-C

http://identifiers.org/hco/9/GRCh38#134830345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27919333-C-A

134830345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27919333-C-G

134830345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27919333-C-T

134830412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919389-G-C

134830487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919462-G-A

134830487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919462-G-T

134830615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919592-T-G

134830834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919775-G-A

134830953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919865-G-A

134831076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27919961-T-A

134831207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920062-C-T

134831353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920156-G-A

134831503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920291-C-T

http://identifiers.org/hco/9/GRCh38#134832603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27920700-C-A

134832636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920725-G-A

134832636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920725-G-T

134832672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920763-T-A

http://identifiers.org/hco/9/GRCh38#134832675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27920766-C-A

134832675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920766-C-T

134832697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920785-C-T

134832707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27920794-A-G

http://identifiers.org/hco/9/GRCh38#134832804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27920893-C-A

134832804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27920893-C-G

http://identifiers.org/hco/9/GRCh38#134832837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27920930-A-C

134832837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27920930-A-G

134832837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27920930-A-T

http://identifiers.org/hco/9/GRCh38#134832847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27920940-C-A

134832877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27920970-G-A

134832877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27920970-G-T

134832968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921042-T-C

134833038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921096-C-T

134833452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921481-G-T

134833472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921500-C-T

http://identifiers.org/hco/9/GRCh38#134833476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27921504-C-A

134833723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921672-C-T

134833762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921702-C-T

134833860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27921769-A-G

http://identifiers.org/hco/9/GRCh38#134834087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27922002-C-A

134834087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922002-C-T

134834096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922012-C-G

134834096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922012-C-T

134834162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922064-G-A

134834191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922091-C-T

134834219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922112-G-A

134834237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922130-C-T

134834246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922139-G-A

http://identifiers.org/hco/9/GRCh38#134834251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27922147-C-A

134834251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922147-C-T

134834617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922322-C-G

134834737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922400-T-A

134834775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922441-G-A

134834819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922463-T-C

134834819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922463-T-G

134834832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922475-G-A

134834832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922475-G-T

http://identifiers.org/hco/9/GRCh38#134834834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27922477-C-A

134834834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922477-C-G

134834834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922477-C-T

http://identifiers.org/hco/9/GRCh38#134834864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27922504-C-A

134834864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922504-C-T

134834871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922511-A-G

134834883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922522-T-A

http://identifiers.org/hco/9/GRCh38#134834943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27922575-C-A

134834943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922575-C-T

134834945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922577-G-A

134834945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27922577-G-T

134835021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27922653-C-G

134835039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27922671-C-T

134838785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27923864-G-C

134839163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27924228-T-A

134839169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27924234-G-A

134839291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27924336-A-G

134839393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27924402-G-T

134839440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27924447-C-T

134839586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27924574-A-G

http://identifiers.org/hco/9/GRCh38#134840852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27925916-C-A

134840896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27925955-T-C

134840982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926053-C-G

134840982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926053-C-T

134840983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926054-G-A

134841298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926337-C-T

134841299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926338-G-A

http://identifiers.org/hco/9/GRCh38#134841881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27926712-C-A

134842021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926798-G-A

134842021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926798-G-T

http://identifiers.org/hco/9/GRCh38#134842024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27926801-C-A

134842024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926801-C-T

http://identifiers.org/hco/9/GRCh38#134842026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27926803-A-C

134842026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926803-A-G

134842026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926803-A-T

134842062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926830-G-T

134842093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926841-A-G

134842094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926842-T-C

http://identifiers.org/hco/9/GRCh38#134842115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27926863-A-C

134842145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27926871-C-T

134842304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927029-G-A

134842304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927029-G-C

134842304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927029-G-T

http://identifiers.org/hco/9/GRCh38#134842622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27927295-C-A

134842622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927295-C-T

http://identifiers.org/hco/9/GRCh38#134842642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27927315-A-C

134842642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927315-A-G

134842684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927352-T-C

http://identifiers.org/hco/9/GRCh38#134843002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27927674-C-A

134843002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927674-C-G

134843002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927674-C-T

134843026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927694-T-C

134843026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927694-T-G

134843226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27927897-A-G

134843563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928214-G-A

134843563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928214-G-T

http://identifiers.org/hco/9/GRCh38#134843671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27928317-C-A

134843671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928317-C-G

134843671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928317-C-T

134843703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928349-T-C

134843814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928483-G-T

134843904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928544-G-T

134843909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928549-G-C

134843909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928549-G-T

134844070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928713-G-T

134844084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928727-G-T

134844154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928777-A-G

134844161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928784-C-T

http://identifiers.org/hco/9/GRCh38#134844164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27928787-C-A

http://identifiers.org/hco/9/GRCh38#134844165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#27928788-C-A

134844165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928788-C-G

134844342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928977-C-T

134844353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27928986-G-T

134844447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27929071-A-G

134844586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27929226-T-C