102293752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124799046-G-C

102294020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124799303-G-A

102294020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124799303-G-T

102294031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124799314-A-G

102294043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 124799327-G-A

102294239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124799494-G-A

102295441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124800437-C-T

102296289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124801213-A-T

102298136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124802020-G-A

102298204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124802080-C-G

http://identifiers.org/hco/13/GRCh38#102298704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124802532-A-C

102298740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124802568-G-A

102298824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124802636-C-T

102298826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124802638-G-A

102298855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124802670-T-C

102299387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124803929-C-G

102299530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124804057-C-G

102299530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124804057-C-T

http://identifiers.org/hco/13/GRCh38#102299537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124804064-A-C

102300209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124804730-G-T

102300512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124804987-T-C

102300633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805096-T-A

102300662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805125-T-C

102300667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805130-G-T

102300858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805341-T-C

102301000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805440-T-A

102301092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805528-C-T

102301102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805538-G-A

102301356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805754-T-C

102301411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 124805808-C-T

102301525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124805925-T-C

102301683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124806077-G-C

http://identifiers.org/hco/13/GRCh38#102303532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124806697-C-A

102303532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124806697-C-T

http://identifiers.org/hco/13/GRCh38#102303774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124806978-C-A

102303774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124806978-C-G

102303774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124806978-C-T

102304102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124807296-T-A

102304553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124807776-A-G

102304794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124807995-G-A

http://identifiers.org/hco/13/GRCh38#102304884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124808072-C-A

102304949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124808145-G-A

102304949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124808145-G-C

102305798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124810303-T-C

http://identifiers.org/hco/13/GRCh38#102306115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124810613-A-C

102306119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124810617-G-C

102306387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124810862-A-G

102308861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124812164-G-A

102309637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124813056-G-A

102309828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124813256-G-A

102310193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124813590-C-T

http://identifiers.org/hco/13/GRCh38#102310745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124813973-C-A

102310745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124813973-C-T

http://identifiers.org/hco/13/GRCh38#102311418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124814635-A-C

http://identifiers.org/hco/13/GRCh38#102311896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124815256-C-A

102312130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124815485-T-C

102312136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124815491-A-G

102312217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124815564-T-A

102312217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124815564-T-C

102312761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124816112-T-C

102312970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124816311-A-G

102313152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124816475-A-G

102313272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124816576-G-A

102313468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124816769-T-C

102314067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124817761-C-T

102314654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124818231-G-A

102314926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124819836-T-G

102315422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124820281-C-T

102315564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124820425-G-A

102315564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124820425-G-T

102316129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124820962-G-A

102317357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124822834-G-A

102317958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124823376-C-G

102317958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124823376-C-T

102317977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124823395-G-A

102318342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124823783-T-C

102318346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124823787-C-G

102318385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124823827-C-T

102319353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124824737-C-T

102319534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124824932-G-A

102319693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124825086-G-A

102319693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124825086-G-T

http://identifiers.org/hco/13/GRCh38#102320103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124825482-A-C

102320209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124825585-C-T

102320366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124825711-T-C

102321097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124829677-T-C

102321428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124830094-T-A

102321428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124830094-T-C

102321467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124830127-G-A

102321467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124830127-G-C

102321470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124830130-C-T

http://identifiers.org/hco/13/GRCh38#102321754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124831000-A-C

102321814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124831060-T-C

102321985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124831520-A-G

102322028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124831566-C-G

http://identifiers.org/hco/13/GRCh38#102322300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124831844-C-A

102322452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124831964-T-C

102322575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124832085-G-A

102322751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124832257-G-A

http://identifiers.org/hco/13/GRCh38#102322881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124832359-C-A

102322881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124832359-C-T

102322969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124832438-G-A

102323113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124832614-A-G

102323138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124832639-A-G

102325735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124833141-A-T

102325857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124833238-G-T

102326284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124833664-A-G

102326929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124834163-C-T

102327227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124834415-T-C

102328583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124837908-C-T

102328690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124838013-G-A

102328852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124838168-C-T

102329536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124838808-C-G

102332319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124841892-C-T

102332540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124842109-T-A

102332754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124842308-T-C

102332891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124842437-A-G

102332901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124842447-C-T

102333764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124843367-G-A

102333764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124843367-G-C

102333935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124843535-T-C

102339809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124847734-A-T

102340141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124847956-C-G

http://identifiers.org/hco/13/GRCh38#102340167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124847982-C-A

102340462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124848304-C-T

102340618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124848445-A-G

102340693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124848516-A-G

102341748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124851798-T-C

102341825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124851869-T-C

102342259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124852252-C-T

102342295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124852287-T-C

102342578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124852527-T-C

102342723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124852583-T-C

102343205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124853132-T-C

102343450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124853344-T-C

102343829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124853698-A-G

102344298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124854351-G-T

102346955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124858998-G-A

102347102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124859132-A-G

102347306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124859368-C-T

102347586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124859588-G-A

102348330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124860616-G-A

102349949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124862645-C-T

102350056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124862768-A-G

102350129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124862842-G-A

102350519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124863280-G-T

102350662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124863411-G-A

102350905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124863613-C-G

102353296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124864595-A-G

102353538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124864817-C-T

102354761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124865226-C-T

102355112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124865533-C-G

102355177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124865597-A-G

102355506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124865856-T-C

102355524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124865874-G-A

http://identifiers.org/hco/13/GRCh38#102355564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124865915-A-C

102356244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124866499-T-C

http://identifiers.org/hco/13/GRCh38#102356296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124866548-C-A

102356296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124866548-C-T

102356312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124866564-T-C

102356888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124867726-A-T

http://identifiers.org/hco/13/GRCh38#102356952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124867794-C-A

102356952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124867794-C-T

http://identifiers.org/hco/13/GRCh38#102356959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124867801-A-C

102356967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124867809-A-G

102357786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124868470-G-A

102357878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124868515-G-A

http://identifiers.org/hco/13/GRCh38#102357985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124868620-C-A

102358057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124868679-T-C

102358586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124869465-G-A

102358586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124869465-G-C

102359708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124874126-A-T

http://identifiers.org/hco/13/GRCh38#102360066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124874496-C-A

102360071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124874501-A-G

http://identifiers.org/hco/13/GRCh38#102364924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124876012-A-C

102364959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124876045-G-T

http://identifiers.org/hco/13/GRCh38#102365043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124876122-C-A

102365043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124876122-C-T

102365140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124876218-C-T

102365276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124876344-T-C

102365949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124877699-A-G

102366211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124877955-T-G

http://identifiers.org/hco/13/GRCh38#102366490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124878826-C-A

102366490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 124878826-C-G

102367125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880304-A-G

102367155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880332-A-G

102367178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880355-G-A

102367178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880355-G-T

102367371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880549-G-A

102367396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880574-A-G

102367412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880590-A-G

102367633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880702-G-A

102367923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880958-C-G

102367923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880958-C-T

102367935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880972-G-A

102367935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124880972-G-T

102368051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881085-G-A

102368051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881085-G-T

http://identifiers.org/hco/13/GRCh38#102368058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124881092-C-A

102368058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881092-C-T

102368093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881100-G-T

102368156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881162-T-C

102368179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881185-A-G

102368314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881320-C-T

102368473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881468-T-C

102368628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124881618-G-A

102368896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882232-G-C

102368896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882232-G-T

102369057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882387-C-T

102369061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882390-C-T

102369125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882420-C-T

102369292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882586-T-G

102369348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882644-C-T

102369536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882822-T-C

102369602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124882883-C-T

http://identifiers.org/hco/13/GRCh38#102374162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124883262-C-A

102374162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124883262-C-T

102374228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124883332-C-T

102374409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124883487-G-A

102374803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124883715-G-A

102374803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124883715-G-T

102375099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124884003-C-T

102375304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124884209-T-G

http://identifiers.org/hco/13/GRCh38#102375373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124884278-C-A

http://identifiers.org/hco/13/GRCh38#102375462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124884347-A-C

102375462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124884347-A-G

102375598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124884499-C-T

102376769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124886358-T-C

102376795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124886384-C-G

102376969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124886937-C-G

http://identifiers.org/hco/13/GRCh38#102376983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124886951-C-A

102376983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124886951-C-T

102377020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124886987-G-A

http://identifiers.org/hco/13/GRCh38#102378715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124888185-A-C

http://identifiers.org/hco/13/GRCh38#102378832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124888295-A-C

102378941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124888388-G-A

102378941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124888388-G-C

http://identifiers.org/hco/13/GRCh38#102379788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124889191-A-C

102379947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124889311-T-A

102379947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124889311-T-C

102379947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124889311-T-G

102380016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124889355-A-G

http://identifiers.org/hco/13/GRCh38#102380497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124889505-A-C

http://identifiers.org/hco/13/GRCh38#102381646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124890821-A-C

102382018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124891201-T-C

102382023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124891206-G-A

102385711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124900388-A-G

102386484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124900696-A-G

102386485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124900697-T-C

102386717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124900926-T-C

102386749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124900958-G-A

http://identifiers.org/hco/13/GRCh38#102387057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124901311-C-A

102387057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124901311-C-G

102390259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124905135-A-G

102391561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124906220-G-C

102391782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124906428-G-A

102391996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124906630-A-G

102392019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124906650-A-G

102392019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124906650-A-T

http://identifiers.org/hco/13/GRCh38#102394475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#124907282-C-A