132954577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23501386-A-T

http://identifiers.org/hco/6/GRCh38#132954604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23501362-A-C

132954820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23498904-A-G

132954902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23498859-T-C

132955036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23498739-G-A

132955116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23496402-A-T

132955194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23496318-G-C

132955199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23496313-G-A

132955345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23496175-T-C

132956796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23494647-C-T

132956989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23494460-A-G

132957340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23494163-T-A

132957340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23494163-T-C

132957581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23493060-G-A

132957799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492877-G-A

132957799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492877-G-T

132957857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492824-G-C

132957985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492703-G-A

132957997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492692-G-A

132958242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492511-G-A

132958352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492418-C-T

http://identifiers.org/hco/6/GRCh38#132958355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23492415-A-C

132958511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492252-A-G

132958705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23492074-T-C

132959288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23491541-G-T

132959936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23490529-C-T

132960262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23490212-T-C

132960445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23490067-A-G

http://identifiers.org/hco/6/GRCh38#132960560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23489947-A-C

132960680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23489843-T-C

132960763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23489749-C-T

132960962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23489554-C-T

http://identifiers.org/hco/6/GRCh38#132961466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23488961-C-A

132961662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23488767-T-C

132961992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23488433-G-A

132961992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23488433-G-T

132962009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23488416-C-T

132962473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487906-T-A

132962604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487799-A-T

132962823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23487576-A-G

132963203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23487233-A-G

132963545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23486853-C-G

http://identifiers.org/hco/6/GRCh38#132963619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23486782-C-A

132963666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23486735-C-T

132963693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23486708-G-A

132963765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23486639-C-T

http://identifiers.org/hco/6/GRCh38#132964010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23486404-C-A

132964316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23486097-G-T

132964447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23485966-A-T

132964554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23485861-A-G

132964657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23485745-C-T

132965023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23485378-G-A

132965236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23485156-A-G

132966179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484373-G-T

132966400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23484117-G-A

132966614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483946-G-T

132966743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483833-T-C

132966795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483795-A-G

132966837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483756-C-T

132966871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483723-C-T

132966927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483671-T-C

132967031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483585-G-C

132967434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483251-G-A

132967434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483251-G-T

132967588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483100-G-A

132967627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483050-T-C

132967630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483047-T-C

132967647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23483030-A-T

132967954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23482747-A-G

132967970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23482732-G-A

http://identifiers.org/hco/6/GRCh38#132968025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23482676-A-C

132969459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23480949-T-C

132969677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23480690-C-G

132969771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23480490-G-A

132970212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23480003-G-A

132970233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23479983-G-A

132970601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23479622-G-T

132970745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23479478-T-C

132970919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23479334-C-T

132971098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23479169-A-G

132971301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23478992-G-A

132971457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23478871-C-T

http://identifiers.org/hco/6/GRCh38#132971681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23478641-A-C

132972437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23477935-G-A

132972731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23477670-A-G

132973252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23477167-A-T

132973896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23476529-A-G

132974051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23476378-G-T

132974053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23476376-A-G

132974461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23475986-G-C

132975753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23475094-T-C

132975769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23475078-A-G

132976043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23474815-A-G

132976098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23474761-A-G

http://identifiers.org/hco/6/GRCh38#132976694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23474512-A-C

132977093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23474106-T-C

132977117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23474083-G-A

132977155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23474045-G-T

132978152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473333-G-A

http://identifiers.org/hco/6/GRCh38#132978209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23473290-C-A

132978291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473218-G-A

132978359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473152-G-T

132978478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473024-G-A

132978478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23473024-G-C

132978814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472735-G-C

132978943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472610-C-G

132979242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472334-T-G

132979259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472318-A-G

132979278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472299-T-C

http://identifiers.org/hco/6/GRCh38#132979585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23472004-A-C

132979589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472000-C-G

132979589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23472000-C-T

132979793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23471782-C-T

132980362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23471022-T-C

http://identifiers.org/hco/6/GRCh38#132980488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23470897-C-A

132980488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23470897-C-T

132980596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23470793-C-T

132980737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23470658-T-C

132980779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23470611-C-T

132980801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23470589-T-C

132980952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23470433-T-C

132987050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23469921-G-A

132987050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23469921-G-T

132987051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23469920-A-T

132987065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23469906-G-A

132987065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23469906-G-C

132987144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23469828-A-T

133011477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23465300-G-T

133011594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23465160-G-A

133011665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23465129-C-T

133011666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23465128-A-G

133011718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23465084-G-T

133011848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23464968-G-T

133011915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23464908-T-C

133011923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23464899-T-A

133013836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463803-G-A

133013836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463803-G-C

133013836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463803-G-T

133013842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463797-A-G

133013842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463797-A-T

133013924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463713-C-T

133013964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463674-G-A

133014038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463594-G-T

133014073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463545-C-T

133014202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463416-A-G

133014289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463331-G-A

133014354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23463261-C-T

133015622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461622-A-G

133015660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461585-G-A

http://identifiers.org/hco/6/GRCh38#133015833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23461440-C-A

133015833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461440-C-T

133015988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461300-A-G

133016078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461226-T-C

http://identifiers.org/hco/6/GRCh38#133016171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23461139-A-C

133016171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23461139-A-T

133016417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460875-T-C

133016702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23460000-C-T

133016906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459838-T-C

http://identifiers.org/hco/6/GRCh38#133016963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23459808-C-A

133017193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459702-T-G

133017237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459655-G-C

133017271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459617-A-G

http://identifiers.org/hco/6/GRCh38#133017324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23459569-C-A

133017324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459569-C-T

133017460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459439-T-C

133017652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459251-G-T

133017658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459245-A-G

133017731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23459200-G-A

133018044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458919-G-T

133018053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458911-T-C

http://identifiers.org/hco/6/GRCh38#133018349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23458642-A-C

133018350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458641-A-G

133018525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458507-C-G

133018525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458507-C-T

http://identifiers.org/hco/6/GRCh38#133018526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23458506-C-A

133018526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23458506-C-G

133028263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23451109-T-G

133028560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450998-G-A

133028560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450998-G-T

133028644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450915-G-A

133028644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450915-G-C

133028657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450902-T-C

133028757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450805-A-T

133028802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450758-C-T

133028839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450720-G-A

133028914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450649-G-A

133028920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450644-G-A

133028920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450644-G-T

133028963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450604-G-A

133029244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450537-G-A

http://identifiers.org/hco/6/GRCh38#133029356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23450433-C-A

133029359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450430-G-A

133029360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450429-T-C

133029430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450362-G-A

133029475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23450322-G-C

133031022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23447444-G-C

133031112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23447356-G-T

133031276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23447212-G-A

133031352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23447139-G-A

133031460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23447074-G-A

133031631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23446886-C-T

133031689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23446830-C-T

133031719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23446800-G-C

133036605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23445882-G-C

133036605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23445882-G-T

133036834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23445707-T-C

133037104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23445474-T-A

133037104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23445474-T-C

133038722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23441896-T-C

http://identifiers.org/hco/6/GRCh38#133039827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23441202-C-A

133040008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23441035-A-G

http://identifiers.org/hco/6/GRCh38#133040179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23440848-C-A

133040313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23440716-C-G

133040335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23440694-A-G

133040464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23440564-A-G

133040674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23440354-G-C

133040820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23440203-C-T

http://identifiers.org/hco/6/GRCh38#133040981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#23440038-C-A

133041074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439951-A-G

133041265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23439799-C-T

133041356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439697-T-C

133041406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439647-A-T

133041430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439623-A-G

133041499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439555-A-G

133041702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439363-G-A

133041805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439263-T-C

133041880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439190-G-A

133041923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23439157-A-G

133042140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23438942-G-C

http://identifiers.org/hco/6/GRCh38#133042195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23438910-C-A

133042517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23438607-C-T

133043134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23437975-A-G

133043220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23437910-T-C

133043272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23437867-G-A

133044407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23436165-T-C

133044441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23436133-C-T

http://identifiers.org/hco/6/GRCh38#133044449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23436125-A-C

133044473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23436096-C-T

133044553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23436011-G-A

133045627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23435171-T-C

133045672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23435136-T-A

http://identifiers.org/hco/6/GRCh38#133046414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23434829-A-C

133046672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23434622-T-G

133046734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23434551-G-T

133046787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23434500-A-G

133046882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23434410-T-A

133046970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23434331-A-G

133047538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433783-C-T

133047600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433733-G-C

133048167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433189-T-C

133049476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431795-C-T

133049499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431770-T-A

133049746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431527-T-C

133050048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431287-C-T

133050069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431277-C-T

133050203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431151-G-A

133050242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431111-T-G

133050310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23431060-C-G

133050729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23430985-C-T

133050899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23430833-T-C

133050950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23430780-G-T

133051003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23430718-C-T

133051089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429886-T-A

133051153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429822-T-A

133051314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429659-T-G

133051341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429632-G-A

133051501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429482-G-A

133051597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429391-G-C

133051671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429332-A-G

133051671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23429332-A-T

133053817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427281-C-G

133054011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23427083-G-A

133054339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426776-T-C

133054362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426753-T-G

133054535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426595-T-G

133054540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426590-T-C

133054603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426520-T-A

133054801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426242-T-C

133054852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426179-G-A

http://identifiers.org/hco/6/GRCh38#133054936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23426097-C-A

133054936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426097-C-T

http://identifiers.org/hco/6/GRCh38#133054968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23426043-A-C

133055043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425972-C-G

133055043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425972-C-T

133055122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425881-T-C

133055123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425880-T-A

133055123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425880-T-C

133055866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23425198-G-A

133056049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425019-A-G

133056229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424850-T-C

133056365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424724-T-C

133056590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424481-G-A

133057012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424089-G-A

133058274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422145-A-G

http://identifiers.org/hco/6/GRCh38#133058290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23422129-C-A

133058471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421947-C-T

133058589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421838-A-G

133058598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421829-A-G

133058617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421810-C-T

133058629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421798-G-A

133058977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421500-C-T

http://identifiers.org/hco/6/GRCh38#133059565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23421388-A-C

133059702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421251-G-A

133059702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421251-G-T

133059737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421214-T-A

133059760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421191-T-C

133059761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421190-T-G

133059764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421187-G-C

133059911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421056-A-G

133059979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420988-A-G

133060001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420967-G-A

133060304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420378-G-A

133060755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420303-T-C

133061109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419938-T-C

133061346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419692-A-T

133061600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419437-A-T

133061865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419179-T-C

133062013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419007-A-G

133062132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418890-G-A

133062201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418824-C-T

133062261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418764-C-T

133062572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418469-A-T

133062580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418454-C-T

133062794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418241-C-T

133062807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418228-T-A

133062833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418202-T-C

http://identifiers.org/hco/6/GRCh38#133062834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23418201-C-A

133062834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418201-C-T

133063035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23418040-G-A

133063038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23418038-G-A

133063304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23417770-C-G

133063359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23417729-G-A

133063441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23417648-C-T

133063501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23417590-C-G

133063506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23417585-T-C

133064456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415575-T-C

http://identifiers.org/hco/6/GRCh38#133064574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23415460-A-C

133064613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415428-G-A

133064614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415427-T-C

133064617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415424-T-C

http://identifiers.org/hco/6/GRCh38#133064666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23415377-A-C

133064688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415355-T-C

133064748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415067-T-A

133064748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415067-T-C

133064863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414953-T-A

133064863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414953-T-C

http://identifiers.org/hco/6/GRCh38#133065007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23414813-C-A

133065007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414813-C-T

http://identifiers.org/hco/6/GRCh38#133065237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23414601-C-A

133065317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414533-G-A

133065361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414488-T-C

133065519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414324-G-A

133065588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414279-C-T

133065632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23414229-T-G

133065901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413974-A-T

133065951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413942-G-A

133065951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413942-G-T

133065958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413935-T-A

133065958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413935-T-C

133066017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413878-G-A

133066017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413878-G-T

133066185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413729-G-A

133066185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413729-G-C

133066271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413648-T-A

133066293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413628-T-C

133066389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413539-T-G

133066419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413517-A-G

133066486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413451-A-T

133066570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413369-T-C

133066594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413344-C-T

133066684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413250-C-T

133068780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412079-A-G

133068953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411895-T-C

133068986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411850-A-T

133069036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411781-T-C

133069140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411568-G-A

133069497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411241-C-T

133070379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408713-C-G

133070379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408713-C-T

133070599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408494-A-G

133070689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408402-G-A

133070982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408105-C-T

133071285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23407740-G-A

http://identifiers.org/hco/6/GRCh38#133071329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23407701-C-A

133071623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23407426-C-T

133071644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23407405-A-G

133072152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405835-T-C

133072697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403592-A-G

133072724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403565-A-G

http://identifiers.org/hco/6/GRCh38#133072798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23403506-C-A

133072798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403506-C-T

133072887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403413-T-C

133073027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403250-G-A

133073436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402849-T-C

133073464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402822-T-C

133073534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402741-T-C

133073588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402689-A-T

133073618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402663-A-T

133073855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402437-T-C

133074024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402054-C-G

133074285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23401803-A-G

133074729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23401408-A-G

133074829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23401284-C-T

133074857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23401262-G-T

133074908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23401215-A-T

133075015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400923-A-G

133075204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400756-G-A

133075204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400756-G-T

133075283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400609-G-A

http://identifiers.org/hco/6/GRCh38#133075397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23400360-A-C

133075596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400185-T-C

133075749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400035-T-C

133075940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399600-G-C

133076138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399406-T-C

133076165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399379-C-G

133076228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399303-C-T

133076318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399221-A-G

http://identifiers.org/hco/6/GRCh38#133076441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23399048-A-C

133076550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23398781-C-T

133078088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397486-G-A

133078088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397486-G-C

133078186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397405-G-T

133078226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397365-G-A

133078226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397365-G-T

133078337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396836-T-A

133078337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396836-T-C

133078382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396793-T-C

133078582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396605-T-C

133078583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396604-A-G

133078596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396592-G-A

133078605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396583-C-T

133078784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396424-T-C

http://identifiers.org/hco/6/GRCh38#133079183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23396030-A-C

133079803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395473-G-T

133079934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395295-C-T

133080042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395198-A-G

133080042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395198-A-T

133080046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395194-G-A

133080059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395181-G-A

133080315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394948-A-G

133080420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394837-A-T

133080624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394627-C-G

http://identifiers.org/hco/6/GRCh38#133080629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23394622-A-C

http://identifiers.org/hco/6/GRCh38#133080817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23394455-A-C

133080833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394439-C-T

133080912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394362-C-G

133081109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394197-A-G

133081201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394098-C-T

133081370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393920-T-C

133081432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393648-C-T

133081466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393587-G-A

133081696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393327-T-C

133081707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393316-T-G

133081732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393296-T-C

133081762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393268-A-G

133081818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393228-A-G

http://identifiers.org/hco/6/GRCh38#133081876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23393171-A-C

133081897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393149-A-G

133082003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393069-A-G

133082140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392948-A-G

133082190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392892-C-G

133083110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392225-T-C

http://identifiers.org/hco/6/GRCh38#133083183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23392174-C-A

133083183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392174-C-G

http://identifiers.org/hco/6/GRCh38#133083232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23392129-C-A

133083232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392129-C-T

133083325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392071-G-A

133083466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391939-A-G

133083641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391778-A-T

133083649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391767-T-C

133083681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391735-A-G

133083700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391717-T-C

133083843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391570-C-G

133083845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391568-G-C

133084106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391313-G-A

133084108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391311-T-C

133084108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391311-T-G

133084239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391184-G-T

133084314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391103-T-C

133084350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391068-A-T

133084352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391066-A-G

133084414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391005-T-C

133084733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390018-T-A

133084980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389762-G-A

133084980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389762-G-C

133084980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389762-G-T

133085066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389678-G-A

http://identifiers.org/hco/6/GRCh38#133085164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23389612-C-A

133085250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389533-T-C

133085260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389523-C-T

133085540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389217-G-A

133085575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389177-G-T

133085593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389159-T-C

133085595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389157-C-T

133086029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388719-T-A

133086029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388719-T-G

133086147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388603-C-T

133086521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388257-C-T

133086575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388208-A-G

133088570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23387696-G-A

133088570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23387696-G-T

http://identifiers.org/hco/6/GRCh38#133088603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23387668-C-A

133088709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387565-G-A

133088709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387565-G-T

133088795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387486-G-T

133088822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23387459-C-T

133088835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23387456-T-C

133088954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23387349-G-A

133089055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23387253-T-C

http://identifiers.org/hco/6/GRCh38#133089103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23387206-C-A

http://identifiers.org/hco/6/GRCh38#133089255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23387047-C-A

133089456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23386849-C-T

133089551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23386756-C-T

133089932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23386358-G-T

133090047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23386249-G-A

133090159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386135-G-T

133090232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386063-C-T

133094986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375701-T-C

133095014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375672-A-G

133095245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375456-A-G

133097878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374315-A-G

133097975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374212-T-A

133098352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23373762-G-T

133098398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23373724-G-T

133098559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373576-A-G

133098581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373557-C-G

http://identifiers.org/hco/6/GRCh38#133099016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23373238-C-A

133099538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23372712-A-G

133099600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23372658-C-T

133099734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372525-C-G

133099825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372438-T-G

133099834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372429-C-T

133099865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372400-G-A

133099865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372400-G-T

133099866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372399-T-A

http://identifiers.org/hco/6/GRCh38#133099898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#23372381-C-A

133099931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372348-G-A

133099931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372348-G-T

133100349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371993-A-G

133104381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369872-T-C

133104420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369832-T-C

133105348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368938-G-A

133105706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368549-G-A

133105751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368504-A-G

133106392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23367349-G-T

133106423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23367312-G-A

133106656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23367135-G-A

133106707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23367085-T-C

133106735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23367061-A-T

http://identifiers.org/hco/6/GRCh38#133106800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#23366996-C-A

133106800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366996-C-G

133106800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366996-C-T

133106879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366928-T-G

133106899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366908-A-G

133107019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366820-C-G

133107019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366820-C-T

133107317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366262-T-A

133107317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41926
most severe consequence: non coding transcript exon variant
orthologous variants: 23366262-T-C