http://identifiers.org/hco/11/GRCh38#119102213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44237808-C-A

http://identifiers.org/hco/11/GRCh38#119102292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44237731-C-A

119102348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 44237675-C-G

119102348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 44237675-C-T

119102405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44237639-G-T

119102419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44237625-G-A

119102419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44237625-G-T

119102695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44237362-A-G

119102923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44237245-A-T

119102961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44237218-C-T

119103417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44236884-C-T

119103718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44236673-A-G

119103886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44236560-G-A

119104059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44236403-C-G

119104451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44236007-T-C

119104673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44235829-T-C

119104694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44235806-C-T

119104731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44235783-C-T

119104809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44235701-G-A

119105154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44233689-G-C

http://identifiers.org/hco/11/GRCh38#119105894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44233061-A-C

119105986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44232977-T-G

119106636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44232262-G-A

119106636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44232262-G-C

119106728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44232170-C-T

http://identifiers.org/hco/11/GRCh38#119106764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44232131-C-A

119106764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44232131-C-T

119106871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44232048-A-G

119107248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44231679-C-T

119107278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44231643-G-T

119107285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44231636-C-G

119107305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44231616-T-C

119107305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44231616-T-G

119107392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44231529-C-T

119107904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 44231021-G-A

119108026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 44230899-C-G

119108026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 44230899-C-T

http://identifiers.org/hco/11/GRCh38#119108036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44230889-C-A

119108036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 44230889-C-T

119108160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230769-T-A

119108160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230769-T-G

119108276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230654-G-A

119108276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230654-G-T

119108333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230598-A-G

119108333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230598-A-T

http://identifiers.org/hco/11/GRCh38#119108352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#44230579-A-C

119108352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 44230579-A-T

119108398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230540-G-A

119108398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230540-G-T

119108402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230536-G-A

119108402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230536-G-T

119108414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230524-G-A

119108414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230524-G-T

119108543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 44230396-G-A

119109956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: 44229121-T-C

119109985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: 44229092-C-T

119110001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: 44229076-G-T

http://identifiers.org/hco/11/GRCh38#119110062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44229015-C-A

119110062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: 44229015-C-T

119110077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: 44229000-G-A

119110077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron variant
orthologous variants: 44229000-G-T

119110191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44228886-C-T

119110275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228816-T-C

119110314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228777-G-A

119110314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228777-G-T

119110318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228773-G-A

119110318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228773-G-T

119110350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228741-T-C

119110350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228741-T-G

119110437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228512-G-T

119110475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228473-G-A

119110475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228473-G-T

119110528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44228446-T-C

119110766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44228208-T-G

119111009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227953-G-A

119111009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227953-G-T

http://identifiers.org/hco/11/GRCh38#119111436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44227592-C-A

119111436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227592-C-T

119111437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227591-C-G

119111437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227591-C-T

119111465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227563-C-G

119111465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44227563-C-T

119111639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227392-A-G

119111640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227391-A-T

http://identifiers.org/hco/11/GRCh38#119111659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44227372-C-A

119111659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227372-C-T

119111714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227308-T-G

http://identifiers.org/hco/11/GRCh38#119111797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44227237-C-A

119111797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227237-C-T

119111822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227213-A-G

http://identifiers.org/hco/11/GRCh38#119111825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44227210-C-A

119111920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227118-A-G

119111920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227118-A-T

119111932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227106-G-T

119112001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227038-G-T

119112003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227036-A-G

119112003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44227036-A-T

119112129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226895-T-C

119112130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226894-G-C

119112130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226894-G-T

http://identifiers.org/hco/11/GRCh38#119112154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44226869-C-A

119112154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226869-C-T

119112175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226848-G-C

119112175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226848-G-T

119112229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226816-T-C

119112499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226552-G-T

119112650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44226403-G-A

119112736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226313-A-T

119112838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226211-A-G

119112933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226144-A-G

119112945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226132-G-T

119112966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226115-T-C

119112995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226079-T-G

119113001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226073-T-A

http://identifiers.org/hco/11/GRCh38#119113009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44226065-C-A

119113009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226065-C-T

http://identifiers.org/hco/11/GRCh38#119113057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44226034-C-A

119113057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44226034-C-T

http://identifiers.org/hco/11/GRCh38#119113109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225995-C-A

http://identifiers.org/hco/11/GRCh38#119113218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225909-C-A

119113218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225909-C-T

http://identifiers.org/hco/11/GRCh38#119113244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225883-C-A

119113244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225883-C-T

http://identifiers.org/hco/11/GRCh38#119113277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225851-A-C

119113277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225851-A-G

http://identifiers.org/hco/11/GRCh38#119113306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225824-A-C

119113306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225824-A-T

http://identifiers.org/hco/11/GRCh38#119113321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225809-C-A

119113321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225809-C-T

http://identifiers.org/hco/11/GRCh38#119113366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225763-C-A

119113366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225763-C-G

119113366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225763-C-T

http://identifiers.org/hco/11/GRCh38#119113391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225749-C-A

119113391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225749-C-G

119113436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225703-G-A

119113436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225703-G-T

119113442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225697-G-A

119113442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225697-G-T

119113444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225695-G-A

119113444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225695-G-T

119113450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225689-T-A

119113450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225689-T-C

http://identifiers.org/hco/11/GRCh38#119113462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225681-C-A

119113462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225681-C-G

119113462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225681-C-T

http://identifiers.org/hco/11/GRCh38#119113480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225663-C-A

119113480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225663-C-G

119113664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44225498-G-A

119113717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225445-G-A

119113761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225403-G-A

119113783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225380-G-T

119113798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225365-C-T

http://identifiers.org/hco/11/GRCh38#119113802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225361-C-A

119113802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225361-C-T

119113816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225347-G-A

http://identifiers.org/hco/11/GRCh38#119113905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44225256-C-A

119113905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44225256-C-T

119114054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44225112-C-T

119114239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44224927-A-G

119114565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44224462-G-T

119114567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44224460-A-G

119114994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44223573-T-C

http://identifiers.org/hco/11/GRCh38#119115137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44223442-C-A

119115243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44223332-A-G

119115243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44223332-A-T

119115480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44223055-T-C

119115506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44223032-T-C

http://identifiers.org/hco/11/GRCh38#119115555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222985-C-A

http://identifiers.org/hco/11/GRCh38#119115613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222931-C-A

119115613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44222931-C-T

119115694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44222859-C-T

119115715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44222838-C-T

http://identifiers.org/hco/11/GRCh38#119115731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222821-A-C

119115731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44222821-A-G

http://identifiers.org/hco/11/GRCh38#119115830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222718-C-A

119115947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44222657-T-A

119115947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44222657-T-G

119116306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222298-C-T

http://identifiers.org/hco/11/GRCh38#119116329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222275-C-A

119116329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222275-C-G

119116329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222275-C-T

119116394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222212-G-A

119116394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222212-G-T

119116420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222186-G-A

119116420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222186-G-T

119116428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222178-T-A

119116428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222178-T-C

http://identifiers.org/hco/11/GRCh38#119116448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222160-C-A

119116448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222160-C-T

119116452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222156-G-A

119116452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222156-G-T

http://identifiers.org/hco/11/GRCh38#119116454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44222154-A-C

119116454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222154-A-G

119116489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222119-A-T

119116510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222098-G-A

119116510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222098-G-T

119116578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44222039-T-A

http://identifiers.org/hco/11/GRCh38#119116643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44221975-C-A

http://identifiers.org/hco/11/GRCh38#119116837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44221782-C-A

http://identifiers.org/hco/11/GRCh38#119116864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#44221755-C-A

119116864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44221755-C-T

119117237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221381-G-T

119117286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221364-T-C

119117298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221355-G-A

119117325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221328-A-G

119117378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221304-C-T

119117399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221283-G-T

119117475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221196-C-T

119117557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29000
most severe consequence: 3 prime UTR variant
orthologous variants: 44221036-G-T