17000739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35847926-T-C

17008813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841090-G-A

17008832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841064-T-G

17008873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35841031-A-G

17009644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35840334-T-C

17009651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35840327-A-T

17009657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35840320-A-G

17009675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35840303-A-G

17010209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35840171-A-G

17010635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35838236-T-A

17010635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35838236-T-C

17012109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35837520-C-T

17012217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35837411-G-A

http://identifiers.org/hco/7/GRCh38#17012474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35837168-C-A

17012477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35837165-G-A

17012602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35837041-A-G

http://identifiers.org/hco/7/GRCh38#17012873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35836789-C-A

17012873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35836789-C-T

17013575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35826061-C-G

17013920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35825784-G-A

17013921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35825783-A-G

17014679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822328-T-A

17014697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822310-T-A

17014697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35822310-T-C

17014956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35821807-T-C

http://identifiers.org/hco/7/GRCh38#17014978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35821785-C-A

17014978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35821785-C-T

17015398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35821459-G-T

17015520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35821346-T-G

17016412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35820728-A-T

17016530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35820623-A-G

17016572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35820586-T-C

17016796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35820377-C-T

17019316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818623-C-G

17019316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818623-C-T

17019390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818545-T-C

17019436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818473-C-T

17019472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818438-A-G

17019522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818394-G-A

17019690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35818017-T-C

17019894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35817841-T-C

17019978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35817753-C-T

17020065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35817653-G-A

17020111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35817625-C-T

http://identifiers.org/hco/7/GRCh38#17020417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35817332-C-A

17020673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817103-G-A

17020673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817103-G-T

17020907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817053-G-A

17020907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817053-G-T

17021011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817028-C-T

17021068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817008-C-T

17021069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35817007-G-A

17021249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35816824-A-G

17021305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35816768-A-T

17021689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35816389-A-G

17021873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35816226-A-G

17022176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815938-T-A

17022179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815935-A-G

17022179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815935-A-T

17022301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815755-C-G

17022349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815671-C-T

17022364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815656-G-A

17022364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815656-G-C

17022364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35815656-G-T

http://identifiers.org/hco/7/GRCh38#17022375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35815651-A-C

17023594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35814255-A-G

17024760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813949-G-T

17024811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813896-T-C

17024929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813781-G-A

17025066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35813607-A-G

17025207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812223-G-A

17025207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812223-G-C

17025336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812100-A-T

17025341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35812095-G-A

17025512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811945-G-A

17025543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811915-G-A

17025543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811915-G-C

17025543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811915-G-T

17025653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811298-A-G

17025818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35811134-A-G

17026059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810893-C-T

17026209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810762-A-G

17026209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810762-A-T

17026349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810631-T-A

17026436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810552-C-T

17026467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810521-G-A

17026483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810507-T-G

17026631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810401-T-C

17026806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810238-A-T

17026919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810121-T-C

17026919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35810121-T-G

http://identifiers.org/hco/7/GRCh38#17027092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35809898-A-C

17027097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35809893-G-T

17028121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806691-T-C

17028209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806605-G-A

17028269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806529-G-C

17028269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35806529-G-T

http://identifiers.org/hco/7/GRCh38#17028384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35806408-A-C

17028968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805812-A-G

17028999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805772-A-G

17029106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805645-A-G

17029287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805431-A-G

17029620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35805069-A-G

17030036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804646-C-G

17030211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804485-T-C

17030360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35804351-C-G

17034176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35801857-A-G

17034585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35801265-T-C

17034896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35801016-T-C

17034934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800977-A-G

17035021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800887-T-C

http://identifiers.org/hco/7/GRCh38#17035089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35800798-C-A

17035418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800470-G-C

17035672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800275-A-G

17035756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800195-A-G

http://identifiers.org/hco/7/GRCh38#17035814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35800138-C-A

17035814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800138-C-G

http://identifiers.org/hco/7/GRCh38#17035815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35800137-C-A

17035815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35800137-C-T

17037262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797674-G-T

17037318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797614-C-G

17037430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797486-G-A

17037468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797444-A-G

17037566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797342-C-T

17037601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797307-G-A

17037605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797303-T-C

17037674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797241-C-T

17037709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35797204-G-T

17038009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796911-T-A

17038143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796776-A-G

17038143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796776-A-T

17038186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796736-C-T

17038194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796728-T-C

17038402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796550-T-A

17038402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796550-T-G

17038417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35796535-C-T

17038635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35795925-A-T

http://identifiers.org/hco/7/GRCh38#17038932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35795354-C-A

17038962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35795319-G-C

17039223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35793200-T-C

17039289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35793135-C-T

17039340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35793085-A-G

17039378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35793048-T-C

17039485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35792946-T-G

17039614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35792828-A-G

17039617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35792825-G-A

17039620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35792822-G-A

http://identifiers.org/hco/7/GRCh38#17039667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35792793-A-C

17039683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35792776-A-G

17039702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35792757-T-C

17040261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35788719-G-T

17040538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35788478-C-T

17040870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35787214-C-T

17041004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35787111-G-C

17041102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35787027-T-C

17041169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35786971-T-C

17041249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786890-A-G

http://identifiers.org/hco/7/GRCh38#17041294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35786843-A-C

17041399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786737-G-A

17041410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786726-A-G

17041562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786574-A-G

17041714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786428-A-T

17042034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786187-T-A

17042034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35786187-T-C

17042251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785980-C-T

17042331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785905-C-G

17042444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785819-C-T

17042497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785770-T-A

17042526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785740-G-C

17042755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785517-T-G

17042907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785384-A-G

17043062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785227-C-T

17043104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35785183-C-T

17043326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784949-T-C

17043389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784888-G-C

17043491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784793-C-T

17043554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784787-C-G

17043554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784787-C-T

17043566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784775-C-T

17043607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784734-T-C

17043628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784713-A-T

http://identifiers.org/hco/7/GRCh38#17043843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35784500-C-A

17044040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35784314-T-G

17044431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35784019-A-G

17044455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35783993-A-T

http://identifiers.org/hco/7/GRCh38#17044520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35783929-A-C

17044647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35783804-G-T

17046904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35783192-T-A

17046905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35783191-C-T

17047015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35782487-G-A

17047015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35782487-G-T

17047188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35782320-A-G

17047393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35782157-C-T

17047448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35782116-G-C

17047667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35781962-T-G

17047765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35781865-A-G

17047867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35781768-G-T

17050287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35777736-A-G

17050338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35777689-C-G

17050338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35777689-C-T

17050500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35777522-T-A

17050503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35777519-T-C

17054335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35777357-C-G

17054335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35777357-C-T

17054336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35777356-G-A

17054627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35777099-C-T

http://identifiers.org/hco/7/GRCh38#17055052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35776722-C-A

17055836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776072-C-T

17055890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35776021-A-G

17056064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35775845-G-T

17056115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35775795-T-C

http://identifiers.org/hco/7/GRCh38#17058295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35771134-C-A

17058390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35771051-A-G

17058570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770892-G-A

17058591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770871-G-T

17058721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770775-A-T

17058734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770762-A-G

17058734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770762-A-T

17058866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770616-T-C

17059017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770463-A-G

http://identifiers.org/hco/7/GRCh38#17059259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35770203-C-A

17059259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770203-C-T

17059301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770161-G-A

17059419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770051-T-A

17059460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770016-G-A

17059460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35770016-G-T

17059534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769943-A-G

17060703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769510-G-A

17061895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35769143-A-G

17063152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768560-G-A

17063158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768554-A-G

17063164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768541-C-T

http://identifiers.org/hco/7/GRCh38#17063295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35768392-A-C

17063295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768392-A-G

17063539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35768146-C-T

http://identifiers.org/hco/7/GRCh38#17063778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35767909-C-A

17063801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767850-T-C

17063892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767759-C-T

http://identifiers.org/hco/7/GRCh38#17063961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35767690-A-C

17064030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767615-A-G

17064056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767588-A-G

17064056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767588-A-T

17064057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767587-T-C

17064151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35767520-C-G

17064322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35766730-A-G

17064333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35766715-A-G

17064373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35766657-A-G

17064863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35765845-C-T

17064985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35765735-A-G

17067365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35764460-G-A

17067435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35764392-C-G

17067458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35764341-C-T

17067460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35764339-C-T

17067660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35764146-G-A

http://identifiers.org/hco/7/GRCh38#17067874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35763974-A-C

17067874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763974-A-G

17068019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763855-A-T

17068290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763574-G-A

17068293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763571-G-C

17068368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763505-T-C

17068690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763435-C-T

17068730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35763393-C-T

17069252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35762975-G-T

17069622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35762569-C-G

17070497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35761783-A-G

http://identifiers.org/hco/7/GRCh38#17070614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#35761672-A-C

17070986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761387-G-T

17071087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35761290-C-T

17071515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760873-T-G

17072057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760195-A-G

17072096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760163-G-A

17072189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35760067-G-A

17072339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759906-T-C

17072481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759779-C-T

17072507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759754-C-T

17072576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759687-A-G

http://identifiers.org/hco/7/GRCh38#17072792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35759332-C-A

17072841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759270-G-T

17072870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759239-T-C

17072881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759228-A-G

17072962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35759155-C-G

http://identifiers.org/hco/7/GRCh38#17072994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35759125-C-A

17073256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35758605-C-G

17073256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35758605-C-T

17073464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35758434-A-G

17073576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757526-G-A

http://identifiers.org/hco/7/GRCh38#17073684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35757423-A-C

http://identifiers.org/hco/7/GRCh38#17073697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35757410-A-C

17073835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757274-A-G

17073857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757256-A-G

http://identifiers.org/hco/7/GRCh38#17073938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35757181-A-C

17074089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35757020-G-A

17074117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756992-A-G

17074166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35756949-A-G

17074955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754544-C-T

17075018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754479-T-A

17075153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754356-T-A

17075375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35754148-A-G

17075613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35753920-C-T

17076043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35753511-C-G

17076045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35753509-G-A

17076352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35753167-C-T

17076435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35753089-C-G

17076523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35753000-T-C

17077486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752696-G-A

17077692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35752493-A-G

http://identifiers.org/hco/7/GRCh38#17079062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35750180-C-A

http://identifiers.org/hco/7/GRCh38#17079107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35750135-A-C

17079180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35750064-T-C

17079404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35749851-G-A

17079414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35749841-A-G

17079526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35749744-A-G

17079527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35749743-T-C

17091384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35747195-A-T

17091395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35747184-C-T

17091439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35747156-C-G

17091566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35747026-T-G

17091719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746889-C-T

17091931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746693-G-A

17091931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746693-G-T

17091944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746682-A-G

17091968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746659-A-G

http://identifiers.org/hco/7/GRCh38#17091969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35746658-C-A

17092088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746536-T-C

17092148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746419-A-G

17092243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746328-T-C

17092341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35746252-C-T

17092778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35745230-A-G

17092868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35745142-T-C

17092871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35745139-A-T

17093194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744834-A-T

17093472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744532-C-T

17093748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744276-G-A

17093831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744201-A-G

17093883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35744147-A-G

17094044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743179-A-G

17094103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743129-G-A

17094137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35743094-A-G

17094477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35742731-C-T

17094571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35742641-T-C

17094730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741473-G-A

17094800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741406-G-T

17094869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741351-C-G

17094887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741337-G-C

17094972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741258-A-G

17095038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741193-G-C

17095137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741096-G-A

17095162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35741071-T-G

http://identifiers.org/hco/7/GRCh38#17095167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35741066-A-C

17095362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35740871-C-T

17095383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35740854-G-A

17095386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35740851-G-A

17095386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35740851-G-T

17098181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35737195-G-A

17098207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35737169-T-C

17098748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35736590-C-G

17098874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35736440-T-A

17099002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35736302-G-C

17099040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35736264-T-C

17099063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35736241-T-C

17099063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35736241-T-G

17099277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35735752-G-A

http://identifiers.org/hco/7/GRCh38#17099359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35735660-A-C

17099796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35735259-T-C

17102778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732383-T-A

17102778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35732383-T-C

http://identifiers.org/hco/7/GRCh38#17102780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35732381-A-C

17103272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731891-A-T

17103536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731665-T-C

17103536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731665-T-G

17103701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731502-G-C

17103708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731496-T-A

17103708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731496-T-C

17103737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731471-A-G

17103938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731314-A-G

17103998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731243-A-G

17104067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35731173-A-T

http://identifiers.org/hco/7/GRCh38#17104364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35730891-A-C

17104383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730873-T-C

17104776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730174-C-T

17104936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35730032-G-A

17105119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35729864-C-G

17105119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35729864-C-T

17105218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35729736-T-G

17120365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35724412-G-A

http://identifiers.org/hco/7/GRCh38#17120566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35724246-C-A

17120588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35724227-G-A

17120617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35724198-T-C

17120821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35724045-A-G

17120826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35724040-T-A

17121958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35723591-G-A

17121958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35723591-G-C

http://identifiers.org/hco/7/GRCh38#17122031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35723513-A-C

http://identifiers.org/hco/7/GRCh38#17122136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35723416-A-C

17122429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35723123-T-A

17122458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35723106-A-G

17122542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35723047-G-A

http://identifiers.org/hco/7/GRCh38#17122708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35722318-A-C

17122708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35722318-A-G

17122759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35722261-A-G

17122766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35722239-A-G

http://identifiers.org/hco/7/GRCh38#17122787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35722218-C-A

17122787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35722218-C-T

17123001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721999-T-A

17123015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721985-T-C

17123091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721910-C-G

17123099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721902-T-C

17123209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721812-G-T

17123325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721690-T-C

17123423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721608-C-T

http://identifiers.org/hco/7/GRCh38#17124025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35721350-A-C

17124025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721350-A-T

17124240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721178-T-C

17124430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721004-A-G

17124432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35721002-A-T

17124589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35720889-G-T

17125051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35717067-T-C

http://identifiers.org/hco/7/GRCh38#17125071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35717048-C-A

17125286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716809-T-C

17125341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716754-A-T

17125512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716600-A-G

http://identifiers.org/hco/7/GRCh38#17125555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35716555-A-C

17125660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716450-T-C

17125708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716405-G-C

17125729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716385-G-A

17125826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716300-G-A

17125863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716265-T-A

17127233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35716044-C-T

17127291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715995-C-T

17127460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715873-T-C

17127525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715817-G-A

17127569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715775-A-G

17127572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715772-C-T

17127689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715694-G-C

17127900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715509-T-G

http://identifiers.org/hco/7/GRCh38#17127991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35715414-A-C

17128071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715345-T-C

17128151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715268-A-G

17128151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715268-A-T

17128174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715245-C-T

17128190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715228-G-A

http://identifiers.org/hco/7/GRCh38#17128565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35715166-A-C

17128754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35715006-T-G

17128833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35714951-G-A

17128833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35714951-G-C

17129934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35713702-C-G

17130036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35713624-A-T

17130113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35713566-A-T

17130194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35713507-T-C

http://identifiers.org/hco/7/GRCh38#17130273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35713422-A-C

17130338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35713358-T-C

17130405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35713293-T-A

17130747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35712968-T-A

17130827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35712897-C-T

17131027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35712679-T-C

17140303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35707052-G-A

http://identifiers.org/hco/7/GRCh38#17140629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35706773-A-C

17140633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35706769-T-C

17140671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35706730-C-T

17144510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702469-C-T

http://identifiers.org/hco/7/GRCh38#17144525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35702454-A-C

17144525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702454-A-G

http://identifiers.org/hco/7/GRCh38#17144560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35702419-C-A

17144561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702418-C-T

http://identifiers.org/hco/7/GRCh38#17144569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35702405-C-A

17144569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702405-C-T

17144582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702392-A-G

17144596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702379-A-G

17144626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702351-C-T

17144677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702312-T-G

17144704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702295-T-C

17144720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35702282-T-C

17144787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35702216-A-G

17144862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35702133-G-T

17146073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700914-G-A

17146076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700911-T-C

17146362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700735-C-G

17146606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700469-T-A

17146606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700469-T-C

http://identifiers.org/hco/7/GRCh38#17146730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35700316-C-A

17146806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700182-G-A

17146806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700182-G-C

17146831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35700153-C-T

17146863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699992-T-C

17146952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699914-A-G

17146952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699914-A-T

17146979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699888-A-G

17146979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699888-A-T

17147156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699717-A-G

17147171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699702-T-A

17147172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699701-C-T

17147266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699613-T-C

17147266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699613-T-G

17147313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699545-T-G

17147588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699280-G-A

17147644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35699229-A-T

http://identifiers.org/hco/7/GRCh38#17148124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35697320-A-C

17156928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35695789-T-C

17157036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35695692-T-C

http://identifiers.org/hco/7/GRCh38#17157320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35695503-C-A

17157709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35695140-C-T

17157710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35695139-G-A

17157710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35695139-G-C

17157733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35695121-G-T

17158604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35694430-G-A

17158843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35691760-C-G

17159619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35691299-C-G

17159619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35691299-C-T

17159714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35691200-C-T

17160015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35690935-A-G

17160037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35690914-T-C

17160070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35690882-G-C

17160070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35690882-G-T

17160249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35690699-A-G

17160970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35690016-C-T

17161099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35689913-T-C

17161219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35689811-T-G

17164667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35689437-G-C

17174069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35687101-G-C

17174096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35687074-G-T

17174171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35687013-A-G

17174469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35686693-G-T

17174535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35686628-C-T

17174716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35686471-A-G

17174807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35686381-C-T

17174820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35686369-C-T

17174851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35686339-G-A

17175065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685808-T-C

17175124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685754-A-G

17175327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685569-G-A

17175377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685528-T-G

17175617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685306-T-A

17175730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685194-G-A

17175735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685189-T-A

17175931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684999-C-T

http://identifiers.org/hco/7/GRCh38#17176031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35684917-A-C

http://identifiers.org/hco/7/GRCh38#17176130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35684828-A-C

17176130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684828-A-G

17176305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684642-G-C

http://identifiers.org/hco/7/GRCh38#17177028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35684308-A-C

17177033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684303-G-A

17177033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684303-G-C

17177035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684301-G-A

17177035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684301-G-T

17177052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684278-G-A

http://identifiers.org/hco/7/GRCh38#17177160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35684185-A-C

http://identifiers.org/hco/7/GRCh38#17177335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35684051-A-C

17177335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684051-A-G

http://identifiers.org/hco/7/GRCh38#17177344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35684042-C-A

17177375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684013-C-T

17177404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683982-C-T

17177546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683850-C-G

17177546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683850-C-T

17177580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683814-C-T

17178028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683419-T-C

17178341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683104-A-G

http://identifiers.org/hco/7/GRCh38#17178415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35683005-A-C

17178419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683001-G-A

17178574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682842-C-T

17178683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682738-C-G

17178702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682719-C-T

17178752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682671-A-G

17178800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682637-A-G

17178949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682488-A-G

17178986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682456-T-G

http://identifiers.org/hco/7/GRCh38#17178989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35682453-A-C

17179294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682170-C-T

17179368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682114-C-T

http://identifiers.org/hco/7/GRCh38#17180271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35681204-C-A

17180292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35681172-A-G

17180426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35681000-T-A

17180600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35680830-T-C

17180660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35680771-T-A

17180702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35680729-T-C

17180924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35680507-G-C

http://identifiers.org/hco/7/GRCh38#17181292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35680173-A-C

17181292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35680173-A-G

17181334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35680132-T-G

17181520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679946-T-C

17181557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679837-C-G

17181712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679639-C-T

17181892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679435-G-A

17181950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679393-T-G

17182045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679318-G-C

17182079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679284-C-T

http://identifiers.org/hco/7/GRCh38#17182317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35679066-C-A

17182317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679066-C-T

http://identifiers.org/hco/7/GRCh38#17182351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35679031-C-A

17182366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35679012-T-C

17182433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35678947-G-A

17182663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677577-G-A

17182663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677577-G-C

17182698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677546-T-C

17182727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677527-T-G

17182815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677434-G-T

17183012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677278-A-G

17183012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677278-A-T

http://identifiers.org/hco/7/GRCh38#17183603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35677037-C-A

17183603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677037-C-G

17183603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677037-C-T

17183624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35677016-A-G

17183663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676981-T-A

17183756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676888-C-T

17183761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676883-T-C

17183879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676775-A-T

17184271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676388-G-A

17184522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35675895-A-G

17184522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35675895-A-T

http://identifiers.org/hco/7/GRCh38#17184816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35675497-C-A

17184816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35675497-C-T

17184820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35675493-A-G

http://identifiers.org/hco/7/GRCh38#17185107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#35675214-A-C

17185385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674951-G-A

17185406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674929-A-G

17185470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674857-G-A

17185634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673965-C-T

17185895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673699-G-A

17185897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673697-T-C

17185941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35673655-G-C

17185941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35673655-G-T

17186112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673487-T-C

17186478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672712-G-A

17186478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672712-G-C

17186550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672641-C-G

17186847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672376-C-G

17186857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672366-C-T

17186861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672362-C-T

http://identifiers.org/hco/7/GRCh38#17186878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35672345-C-A

17186904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672321-C-T

17186975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672252-T-C

17187144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672100-C-T

17187263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671990-C-T

17190832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671696-T-A

17190871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671659-A-G

17190885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671645-C-T

17191079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671473-C-G

17191200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671362-A-G

17191204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35671358-G-A

17191786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35670202-G-A

17191787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35670201-C-T

17191889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35670111-T-C

17192059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669941-C-G

17192064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669936-C-G

17192068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669932-G-A

17192068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669932-G-T

17192078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669922-G-A

17192109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669891-T-G

17192301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669545-A-G

17192332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669516-A-G

17192356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669492-T-C

17192550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35667090-T-C

17192592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35667043-G-A

17192714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666933-C-T

17192746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666906-G-T

http://identifiers.org/hco/7/GRCh38#17193961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35666672-C-A

17194010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666634-T-A

17194010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666634-T-C

http://identifiers.org/hco/7/GRCh38#17194014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35666630-A-C

17194110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666540-C-T

17194120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666531-G-T

17194217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666440-G-A

17194217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666440-G-C

17194238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666418-G-A

17194445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666228-T-G

17194544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666142-A-G

17194586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666093-C-T

17194622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666058-T-G

17194778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35665898-T-C

17195217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35665491-A-G

17195250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35665466-T-A

17195250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35665466-T-C

17195892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35664949-C-T

17195924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35664916-C-T

http://identifiers.org/hco/7/GRCh38#17195940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35664902-A-C

17196173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35664673-A-G

17196294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35664561-A-G

17196354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35664500-A-T

17197856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35663840-T-C

17198191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35663541-T-C

17198602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35658596-A-G

17198749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35658448-A-G

17198898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35658269-T-G

17199546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657656-G-A

17199546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657656-G-C

17199546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657656-G-T

17199667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657490-G-A

17199667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657490-G-C

17199740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657419-A-G

http://identifiers.org/hco/7/GRCh38#17199812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35657352-C-A

17199866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656443-T-C

17199926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656386-G-A

17200011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656210-G-A

17200011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656210-G-T

17200117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656101-C-T

17200141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656077-T-C

17200405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35655836-C-T

http://identifiers.org/hco/7/GRCh38#17200458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35655785-A-C

17203640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35652268-A-T

17203937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35652009-G-A

17203997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651950-T-C

17203998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651949-A-G

17204118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651854-C-T

17204158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651841-T-C

17204946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651271-G-A

17205306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651154-T-C

17205498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651014-G-A

17205642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35650879-A-T

17206144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35649827-C-G

17206253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35649723-A-T

17206420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35649471-G-A

17206420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35649471-G-C

http://identifiers.org/hco/7/GRCh38#17206706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#35649199-C-A

17206706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35649199-C-T

17206756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35649144-C-T

http://identifiers.org/hco/7/GRCh38#17206873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35649037-A-C

17206873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35649037-A-G

17206932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648978-A-G

17207096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648837-G-A

17207121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648820-G-A

17207298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648663-C-T

17207371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648589-G-A

17207372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648588-C-T

17207634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648360-A-G

17207728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35648262-A-G

17208058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35647176-T-G

17208114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35647125-T-C

17208121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35647118-G-A

http://identifiers.org/hco/7/GRCh38#17208192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35647047-C-A

17208207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35647032-G-T

17208387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35646882-A-T

17208449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35646809-A-G

17208488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35646770-T-G

17210385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35643180-T-C

17210653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642773-G-A

17210889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642554-G-A

17210918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642532-C-G

17210924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642526-T-C

17210929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642521-T-G

17210946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642504-G-C

17211063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642420-C-T

17211090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642396-A-G

17211222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642290-A-T

17211466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35642058-T-G

17212398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35641467-G-A

17212448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35641421-T-A

17212448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35641421-T-C

http://identifiers.org/hco/7/GRCh38#17213005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35640933-A-C

17213027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640919-C-T

17213054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640894-T-C

17213464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640489-C-T

17213467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640486-A-T

17213471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640420-C-T

17213820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640063-T-G

17222579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638765-C-G

17222691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638676-G-A

17222718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638651-A-G

17222761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638607-G-A

17223001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638404-A-T

17223011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638394-A-T

17223207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638205-T-C

17223239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638182-T-A

17223834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35636233-T-C

17226601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35634782-T-C

17226604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35634779-C-T

http://identifiers.org/hco/7/GRCh38#17226929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35634477-A-C

17226975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35634431-G-A

17226975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35634431-G-C

17227025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35634378-C-T

http://identifiers.org/hco/7/GRCh38#17227050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35634325-C-A

17227064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35634312-G-T

17227075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35634301-G-T

http://identifiers.org/hco/7/GRCh38#17227106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35634275-A-C

http://identifiers.org/hco/7/GRCh38#17227262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35634117-C-A

17227283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35634098-T-C

17227414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633972-T-G

17227475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633910-A-G

http://identifiers.org/hco/7/GRCh38#17227506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35633875-A-C

17227653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633728-A-G

17227686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633695-A-G

http://identifiers.org/hco/7/GRCh38#17227891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35633562-A-C

17227891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633562-A-G

17227899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633554-G-C

17227985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633480-T-C

17228029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633445-G-A

17228038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633436-A-G

17228072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633338-G-A

17228412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35633028-A-T

17228444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35632996-C-T

17230311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632847-A-G

17230365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632793-G-C

17230376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632783-G-A

17230384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632775-G-C

17230396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632764-T-A

17230609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632571-G-A

17230750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632444-G-A

17230828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632366-T-C

17230998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632182-T-G

17231099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632093-T-C

17231144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632054-T-C

17231182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632017-C-G

17231261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631964-T-C

17231268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631957-T-A

17231338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631894-G-A

17231338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631894-G-T

17231354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631878-A-G

http://identifiers.org/hco/7/GRCh38#17231358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35631874-C-A

17231358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631874-C-G

17231440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631791-G-A

17231987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631390-C-T

17232030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631348-A-G

17232058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631320-C-G

17232058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631320-C-T

17232097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631278-C-T

17232113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631262-C-T

17232194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631212-G-A

17232194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631212-G-T

17232384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631046-G-A

17232903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35630719-G-C

17232903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35630719-G-T

17233149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35630386-G-A

http://identifiers.org/hco/7/GRCh38#17233715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35629859-A-C

17233966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35629669-T-C

17234518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35629195-G-A

17234587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35629113-G-A

http://identifiers.org/hco/7/GRCh38#17234661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35629041-C-A

17234708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35628994-T-C

http://identifiers.org/hco/7/GRCh38#17234755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35628948-A-C

17235176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35628530-T-C

17235212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35628489-G-C

17235983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35627072-T-C

17236224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626868-G-A

17236422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626679-C-G

17236613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626469-C-T

17236671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626402-C-G

17236671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626402-C-T

17236747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626318-G-A

17236772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626299-T-C

17236849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35626222-A-T

http://identifiers.org/hco/7/GRCh38#17236930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35626073-C-A

17237034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625959-C-G

17237196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625791-T-C

17237279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625707-C-G

17237279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625707-C-T

http://identifiers.org/hco/7/GRCh38#17237317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35625671-C-A

17248196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35624247-A-G

17248254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35624189-A-G

17248424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35624020-T-A

17248680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623774-C-T

17248683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623771-G-A

17248697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623757-G-A

17248859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623596-A-T

17248901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623554-C-T

17249016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623437-T-A

17249016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623437-T-G

17249027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623426-C-T

17249034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623419-C-G

17249034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623419-C-T

17251756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35621234-C-T

17251839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35621150-A-G

17252139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35620825-A-G

17252153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35620811-T-G

http://identifiers.org/hco/7/GRCh38#17252994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35620433-A-C

17252994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35620433-A-T

17253216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35620201-C-T

17254289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35619928-T-G

http://identifiers.org/hco/7/GRCh38#17254668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35619535-A-C

17255318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35619189-A-T

17255372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35619135-A-T

http://identifiers.org/hco/7/GRCh38#17255419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35619090-A-C

17255422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35619087-G-C

http://identifiers.org/hco/7/GRCh38#17255732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35618800-A-C

17255732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35618800-A-G

17255797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35618731-T-C

17255926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35618610-A-G

http://identifiers.org/hco/7/GRCh38#17256018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35618539-A-C

17256691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35617294-T-G

17257147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616828-G-A

17257205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616775-G-A

17257282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616697-A-G

17257332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616657-G-A

17258691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616216-A-G

http://identifiers.org/hco/7/GRCh38#17258891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35615503-A-C

17259354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35615141-G-A

17259363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35615132-A-G

http://identifiers.org/hco/7/GRCh38#17259451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35615050-C-A

17259505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614993-G-A

17259585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614946-G-A

17259745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614771-G-C

17259745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614771-G-T

17259790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614719-C-G

17259790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614719-C-T

17259961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614547-C-G

17259997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614512-C-T

17259998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614511-C-G

17260159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35614216-G-C

17260477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613915-T-A

17260600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613792-T-A

17260616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613776-G-T

17260930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613465-T-C

17261164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613236-T-A

17261164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613236-T-C

17261510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35612929-T-C

17261603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35612838-T-A

17261615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35612833-T-C

17262337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35609990-T-G

17262422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35609909-A-G

17262511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35609806-A-G

17262592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35609726-A-G

17262593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35609725-T-A

17272602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35608693-T-G

17272635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35608663-T-G

17272732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35608574-C-T

17272765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35608553-C-T

http://identifiers.org/hco/7/GRCh38#17272780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35608538-C-A

17272795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35608523-A-T

17273723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606898-T-A

http://identifiers.org/hco/7/GRCh38#17273759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35606864-A-C

17273776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606846-T-C

17274963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605954-C-T

17275028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605887-T-C

17275072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605846-T-A

17275129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605799-G-C

17275136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605795-T-C

17275158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605773-T-G

http://identifiers.org/hco/7/GRCh38#17275648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35604454-C-A

17275914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604192-T-C

17276154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35603980-G-T

17276155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35603979-C-T

17276185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603951-T-G

17276397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35603772-G-A

17276574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603601-C-G

http://identifiers.org/hco/7/GRCh38#17276718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35603477-A-C

17276828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603405-T-G

17277167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603231-G-A

17277395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603018-A-G

17277520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35602915-C-T

http://identifiers.org/hco/7/GRCh38#17277549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35602882-A-C

http://identifiers.org/hco/7/GRCh38#17277651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35602798-C-A

17277651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35602798-C-T

http://identifiers.org/hco/7/GRCh38#17278845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35600836-A-C

17279022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600684-G-C

17279040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600666-T-C

17279079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600629-C-T

17279126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600604-A-T

17279205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600540-T-C

17279309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600450-A-G

17279319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600440-C-T

17279342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600417-G-A

17279409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600361-A-G

http://identifiers.org/hco/7/GRCh38#17279436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35600332-A-C

17279614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600219-G-C

17279742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35600130-G-A

17282245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595911-C-T

17282247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595909-G-T

17282584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595573-T-C

17282893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595277-T-C

17282989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595202-G-A

17288373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35594023-A-G

17288378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35594018-T-C

17288464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593932-G-A

17288661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593739-T-C

17288890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593534-G-A

http://identifiers.org/hco/7/GRCh38#17289101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35593325-C-A

17289243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593230-T-A

http://identifiers.org/hco/7/GRCh38#17289472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35593007-A-C

17289593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35592888-T-C

17292384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35591985-A-G

17292442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 35591922-T-G

17292469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591895-A-G

17292536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591846-T-C

17292538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591844-T-C

http://identifiers.org/hco/7/GRCh38#17292556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35591826-C-A

17292556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591826-C-G

http://identifiers.org/hco/7/GRCh38#17292864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35591434-A-C

17292946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591348-G-A

17292946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591348-G-T

http://identifiers.org/hco/7/GRCh38#17293091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35591223-C-A

17294387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35590688-G-C

17294651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35590435-T-C

17294696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35590386-A-G

17294867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35590057-C-G

17295016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589869-A-G

17295055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589831-G-T

17295218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35589690-C-T

17295413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35589483-C-T

17295415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35589481-T-C

17295699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35589242-G-A

17295923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35589058-G-T

17295951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35589031-G-A

17296003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588988-C-T

http://identifiers.org/hco/7/GRCh38#17296074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35588919-C-A

17296182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588817-G-A

17296182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588817-G-C

17296193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588815-T-C

17296426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588681-T-C

http://identifiers.org/hco/7/GRCh38#17296451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35588656-C-A

17296451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588656-C-T

17296560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588559-G-T

17296608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588498-C-G

17296608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588498-C-T

17296742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588364-A-G

17296791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588316-T-A

17296791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588316-T-C

17296794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588313-G-C

17296894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588253-A-G

17296965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35588182-A-G

17297180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35587956-T-C

http://identifiers.org/hco/7/GRCh38#17297358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35587757-C-A

17297455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587673-C-T

17297490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587640-G-A

17297490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587640-G-C

17297569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587579-C-T

17297590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587482-C-T

17297654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587379-T-C

17297759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587278-T-C

17297775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35587262-T-C

17298247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585408-G-A

17298251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585398-T-C

17298257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585392-A-G

17298257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585392-A-T

17298262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585387-T-C

17298263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585386-C-T

17298265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585384-C-T

17298372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35585295-T-G

17298424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35585254-T-A

17298424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35585254-T-C

17298424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35585254-T-G

17298642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585001-G-A

17298642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585001-G-T

17298647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35584996-G-A

17298669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584972-G-A

http://identifiers.org/hco/7/GRCh38#17298714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35584925-A-C

17298714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584925-A-G

http://identifiers.org/hco/7/GRCh38#17298822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35584824-A-C

17298822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584824-A-G

17298822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584824-A-T

17298824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584822-C-T

17298834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584816-C-T

http://identifiers.org/hco/7/GRCh38#17298963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35584747-C-A

17298963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584747-C-T

http://identifiers.org/hco/7/GRCh38#17298967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35584743-C-A

17298967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584743-C-G

17298967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35584743-C-T

http://identifiers.org/hco/7/GRCh38#17298970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35584740-C-A

17299148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35584640-G-T

17299428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584494-G-A

17299428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584494-G-C

17299428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584494-G-T

17299545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584459-C-T

17299554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584450-C-T

17299559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584445-G-T

17299619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584405-T-C

17299888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584141-G-A

http://identifiers.org/hco/7/GRCh38#17300041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35584005-A-C

http://identifiers.org/hco/7/GRCh38#17300196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35583815-C-A

17300200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583811-T-A

17300203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583808-T-G

17300254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583755-G-C

17300333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583688-T-C

http://identifiers.org/hco/7/GRCh38#17300366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35583659-C-A

17300638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583354-C-G

17300870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583124-T-C

17301013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582971-A-G

17301079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582900-T-A

17301179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582794-A-G

17301588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582438-T-C

17302027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582023-C-G

http://identifiers.org/hco/7/GRCh38#17302180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35581900-A-C

17302180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35581900-A-T

17302325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35581795-A-G

17302459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35581653-A-G

17302589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35581519-C-G

17302633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35581494-A-G

17303174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580900-C-T

17303425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580625-T-A

17303436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580614-A-T

http://identifiers.org/hco/7/GRCh38#17303535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35580519-C-A

17303734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580340-A-G

17303805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580266-G-A

17303948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580136-T-C

17303963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35580121-A-G

17304257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579885-T-G

17304477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579678-C-G

17304477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579678-C-T

17304489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579666-T-C

http://identifiers.org/hco/7/GRCh38#17304608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35579566-C-A

17304608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579566-C-T

http://identifiers.org/hco/7/GRCh38#17304610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35579564-C-A

17304610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579564-C-T

17304623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579563-A-G

17304643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579542-G-C

http://identifiers.org/hco/7/GRCh38#17304816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35579399-A-C

17305124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35579161-C-T

17309852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576939-A-G

17309852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576939-A-T

17309862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576929-A-G

17310012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35576789-G-A

17310206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576585-A-G

17310214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576577-T-C

http://identifiers.org/hco/7/GRCh38#17310238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35576547-C-A

17310295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576494-C-T

http://identifiers.org/hco/7/GRCh38#17310374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35576417-C-A

17310374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576417-C-T

17311957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35574102-T-A

17312120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35574001-C-T

17312166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35573970-A-G

17312166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35573970-A-T

17312174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35573962-C-T

17312319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573830-T-C

17312358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573788-T-A

17312730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573506-T-G

17312794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573441-G-A

17312855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573380-G-A

17312855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573380-G-C

17313000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573233-C-T

17313819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35572448-A-T

17313905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35572365-A-G

17316934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35571376-G-C

17317063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35571259-A-G

17317110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35571217-A-T

17317190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35571154-G-T

17317335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35571012-G-C

17317657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570719-A-G

17317897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570500-T-A

17317918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570479-T-C

17318063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569762-G-T

17318113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569712-T-C

17318206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569619-T-C

17318319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569556-C-T

17318338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569538-A-G

17318340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569536-G-A

http://identifiers.org/hco/7/GRCh38#17318361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35569515-A-C

17318623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569287-C-T

17318629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569281-C-T

http://identifiers.org/hco/7/GRCh38#17318678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35569226-C-A

17319213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569003-G-A

17319213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569003-G-T

17319299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568939-C-T

17319331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568907-C-T

http://identifiers.org/hco/7/GRCh38#17319609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35567071-A-C

17319618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35567058-G-T

http://identifiers.org/hco/7/GRCh38#17319732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35566973-A-C

17319737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566968-G-A

17319820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566887-A-G

17319826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566881-T-A

17320146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566586-C-G

17320217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566522-T-C

17320689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566061-A-G

17320729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566018-C-T

17320783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565965-G-T

17320991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565752-C-G

17321375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565437-T-C

17321389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565422-A-G

17321428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565383-T-C

http://identifiers.org/hco/7/GRCh38#17321431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35565380-C-A

17322576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35565049-T-C

17322576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35565049-T-G

17323229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35564770-A-G

17323418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35564579-A-T

17323514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35564478-G-C

17326956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35563667-A-G

17327626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35563086-T-C

17327637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35563074-T-A

17327637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35563074-T-G

17327753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 35562951-T-C

17327837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35562867-G-A

17327837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35562867-G-T

17327860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562844-T-A

17327860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562844-T-C

17327875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562822-A-G

17327875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562822-A-T

17327889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562808-T-C

17328006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562717-T-A

17328043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562688-A-G

17328043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562688-A-T

17328100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562540-G-A

17328247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562397-T-A

17328247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562397-T-G

http://identifiers.org/hco/7/GRCh38#17328302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35562342-A-C

17328493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562112-T-G

17328528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562074-G-C

17328672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561942-T-A

17329716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561349-G-A

http://identifiers.org/hco/7/GRCh38#17329717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35561348-C-A

17329719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561346-T-C

http://identifiers.org/hco/7/GRCh38#17329732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35561333-C-A

17329732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561333-C-T

17329946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35561173-C-T

17330015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35561104-C-T

17330191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35560955-G-A

17330434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35560384-G-C

17330634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35560193-A-G

http://identifiers.org/hco/7/GRCh38#17330715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35560129-C-A

17330781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35560068-A-G

http://identifiers.org/hco/7/GRCh38#17330799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35560050-C-A

17330799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35560050-C-G

17330799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35560050-C-T

17330822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35560027-C-T

17330842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35560007-A-G

17331730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35559166-C-T

http://identifiers.org/hco/7/GRCh38#17331933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35559033-A-C

17331952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35559013-G-C

17333338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558856-T-G

17333380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558815-A-G

17333559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558665-G-A

17333559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558665-G-T

17333601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558612-A-G

17333679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558539-G-A

17333764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558462-G-A

17333764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558462-G-C

17333865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35558363-A-G

17334084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35558157-T-C

http://identifiers.org/hco/7/GRCh38#17334124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35558118-A-C

17334128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558114-T-C

http://identifiers.org/hco/7/GRCh38#17334175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35558078-C-A

17334175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558078-C-T

http://identifiers.org/hco/7/GRCh38#17334186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35558067-A-C

17334188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558065-A-T

17334509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557846-T-C

17334644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557731-G-T

17334750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557622-A-G

17334763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557609-A-G

17334936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35557477-T-A

17334983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35557430-G-C

17334991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35557422-T-C

http://identifiers.org/hco/7/GRCh38#17334992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35557421-C-A

17334992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35557421-C-G

17334992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35557421-C-T

17335079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35557165-G-T

17335103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35557145-A-G

17335103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35557145-A-T

17335189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35557061-T-C

http://identifiers.org/hco/7/GRCh38#17335559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35556726-C-A

17335559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35556726-C-T

17335604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35556439-A-G

17335766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35556262-T-C

17335815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35556214-A-G

17335842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35556187-T-C

17335925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35556108-A-G

17335937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35556096-T-C

17336225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555867-A-G

17336254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555832-T-C

17336301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555784-A-G

17336556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555503-T-A

17336879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555244-A-G

17338907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555055-G-A

17338921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555041-A-T

17338935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555027-T-A

17338935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35555027-T-C

17339147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554812-C-G

17339147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554812-C-T

17339210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554749-A-G

17339230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554729-C-G

17339259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35554709-T-C

17339330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554638-C-G

17339330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554638-C-T

http://identifiers.org/hco/7/GRCh38#17339404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35554561-C-A

17339404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35554561-C-T

17339445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35554520-C-T

17339576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35554383-A-G

17339576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35554383-A-T

http://identifiers.org/hco/7/GRCh38#17339608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35554351-A-C

17339614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35554345-T-G

17339677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35554285-C-T

17339843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35554092-A-G

17340001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35553934-C-G

http://identifiers.org/hco/7/GRCh38#17340085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35553853-C-A

17340085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35553853-C-T

17340091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35553847-T-G

17340188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35553750-A-G

http://identifiers.org/hco/7/GRCh38#17340257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35553682-C-A

17340257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553682-C-T

17341236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553258-G-A

17341236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553258-G-C

17341271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553216-C-T

17342561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35551015-A-G

17342673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550929-T-G

17342852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550756-T-C

17342853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550755-G-A

17342853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550755-G-T

17342871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550743-A-G

http://identifiers.org/hco/7/GRCh38#17342971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35550644-A-C

17343047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35550574-T-C

17343138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550507-A-G

17343217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550461-G-A

17343217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550461-G-T

17343286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550402-T-C

17343286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550402-T-G

17343330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550375-G-A

17343330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550375-G-T

http://identifiers.org/hco/7/GRCh38#17343343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35550362-A-C

17343359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550347-G-T

http://identifiers.org/hco/7/GRCh38#17343491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35550233-A-C

17343491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35550233-A-T

17343811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35549890-A-G

17343811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35549890-A-T

17343898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35549804-T-C

17344034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35549674-A-T

17344098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35549607-T-G

http://identifiers.org/hco/7/GRCh38#17344593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35549150-C-A

17345149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35548931-T-A

17345155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35548924-A-G

17345432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35548687-C-T

17345522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35548600-G-T

17345772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35548348-T-C

http://identifiers.org/hco/7/GRCh38#17345989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#35548139-C-A

17345989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 348
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35548139-C-T