81189654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3 prime UTR variant
orthologous variants: 119955319-A-G

81189758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3 prime UTR variant
orthologous variants: 119955443-G-A

81189775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 119955467-G-T

http://identifiers.org/hco/17/GRCh38#81189779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119955471-C-A

81189779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 119955471-C-T

http://identifiers.org/hco/17/GRCh38#81189838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119955530-C-A

81189838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: 119955530-C-T

81189867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119955556-G-A

http://identifiers.org/hco/17/GRCh38#81189955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119955651-C-A

81189955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 119955651-C-T

81189966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 119955662-T-C

81189994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119955689-A-G

http://identifiers.org/hco/17/GRCh38#81190008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119955703-C-A

81190008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119955703-C-T

http://identifiers.org/hco/17/GRCh38#81190011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119955706-C-A

81190434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956072-C-G

http://identifiers.org/hco/17/GRCh38#81190536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119956136-C-A

81190536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956136-C-T

http://identifiers.org/hco/17/GRCh38#81190604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119956187-C-A

81190604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956187-C-T

http://identifiers.org/hco/17/GRCh38#81190605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119956188-C-A

81190605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956188-C-T

81190794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119956369-C-T

81190875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956420-G-A

81190875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956420-G-T

http://identifiers.org/hco/17/GRCh38#81190885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119956429-C-A

81190885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956429-C-T

81190907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 119956464-C-T

http://identifiers.org/hco/17/GRCh38#81191158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119956700-C-A

81191179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956723-T-C

81191193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 119956737-C-T

81191297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119956841-T-C

81191300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119956844-C-T

http://identifiers.org/hco/17/GRCh38#81191399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119956956-C-A

81191399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119956956-C-T

81191441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957004-A-G

81191443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957006-C-G

81191510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957074-G-A

81191522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957086-G-A

81191538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957098-T-A

81192033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957323-C-T

81192039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957329-G-C

81192068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957357-C-T

81192108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957391-T-C

81192112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957395-T-G

81192381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119957583-A-G

81192401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957605-C-G

81192401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957605-C-T

http://identifiers.org/hco/17/GRCh38#81192453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119957715-A-C

http://identifiers.org/hco/17/GRCh38#81192457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119957718-C-A

81192457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957718-C-G

81192471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957732-T-C

81192580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119957851-G-T

81192626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119957897-T-C

81192789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119958009-C-T

81192809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119958029-G-A

81192809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, missense_variant
orthologous variants: 119958029-G-T

81192917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958105-G-T

81193010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958174-G-A

81193424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958419-G-A

81193697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958658-G-A

81193766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958730-G-A

http://identifiers.org/hco/17/GRCh38#81193777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119958734-C-A

81193777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958734-C-T

http://identifiers.org/hco/17/GRCh38#81193803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119958760-C-A

81193803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119958760-C-T

http://identifiers.org/hco/17/GRCh38#81194003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119958849-C-A

81194003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119958849-C-G

81194003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119958849-C-T

81194074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense_variant, undefined
orthologous variants: 119958920-T-C

81194074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous_variant, undefined
orthologous variants: 119958920-T-G

81194123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119958969-C-T

http://identifiers.org/hco/17/GRCh38#81194135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119958983-C-A

81194135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119958983-C-G

81194135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119958983-C-T

http://identifiers.org/hco/17/GRCh38#81194580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119959357-A-C

81194813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959477-G-A

81194813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959477-G-T

81194854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959508-G-T

81194857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959511-G-T

81194898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119959552-G-A

http://identifiers.org/hco/17/GRCh38#81194976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119959630-C-A

81194976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119959630-C-G

81194976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119959630-C-T

81195043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959659-A-G

http://identifiers.org/hco/17/GRCh38#81195059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119959673-C-A

81195071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959685-G-A

81195071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959685-G-T

81195111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959705-A-G

81195111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959705-A-T

http://identifiers.org/hco/17/GRCh38#81195123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119959717-C-A

81195123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119959717-C-T

81195483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119960664-A-T

81195622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119960794-G-A

81195707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119960914-G-A

81195707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119960914-G-T

http://identifiers.org/hco/17/GRCh38#81195716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119960923-C-A

81195716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119960923-C-T

http://identifiers.org/hco/17/GRCh38#81195761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119960974-C-A

81195761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119960974-C-T

81195805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961061-G-A

81195818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961075-A-G

81195827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119961089-A-G

81195901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961181-G-A

81195901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961181-G-C

81195901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961181-G-T

81195946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961226-A-T

81195959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119961239-G-A

81195959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119961239-G-T

81196683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961296-G-A

81196683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961296-G-C

81196683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961296-G-T

81196748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119961358-C-T

http://identifiers.org/hco/17/GRCh38#81196830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119961440-C-A

81196830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119961440-C-T

81196831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119961441-A-G

81196831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119961441-A-T

81196835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961445-T-A

81196838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961448-G-T

81196866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961501-T-C

81196903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961536-C-G

81196903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961536-C-T

81196913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961578-A-T

81196914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961579-G-A

81196999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961687-C-T

81197011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961699-G-A

81197011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961699-G-C

81197011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961699-G-T

http://identifiers.org/hco/17/GRCh38#81197047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119961720-C-A

81197047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961720-C-G

81197047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119961720-C-T

81197123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961782-T-C

81197170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961828-G-A

http://identifiers.org/hco/17/GRCh38#81197175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119961833-C-A

81197175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961833-C-T

81197180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961838-G-C

81197180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961838-G-T

81197220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961883-G-A

81197246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961905-G-C

http://identifiers.org/hco/17/GRCh38#81197250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119961909-C-A

81197250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961909-C-G

81197250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961909-C-T

81197284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961938-A-G

http://identifiers.org/hco/17/GRCh38#81197285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119961939-A-C

81197285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961939-A-G

81197285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119961939-A-T

81197357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119962013-T-C

81197357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119962013-T-G

http://identifiers.org/hco/17/GRCh38#81197386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962034-A-C

81197386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119962034-A-G

81197386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119962034-A-T

http://identifiers.org/hco/17/GRCh38#81197525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962084-C-A

81197525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962084-C-T

http://identifiers.org/hco/17/GRCh38#81197632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962147-C-A

81197632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962147-C-T

http://identifiers.org/hco/17/GRCh38#81197679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962168-C-A

81197679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962168-C-T

81197702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962175-G-T

81197757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119962230-G-A

81197832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119962305-A-G

81197841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119962314-T-G

81197968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962433-G-A

81197968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962433-G-T

81198000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962472-A-G

http://identifiers.org/hco/17/GRCh38#81198293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962881-A-C

81198306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962901-G-T

http://identifiers.org/hco/17/GRCh38#81198381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962950-C-A

81198381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962950-C-T

http://identifiers.org/hco/17/GRCh38#81198436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119962987-C-A

81198436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962987-C-G

81198436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119962987-C-T

81198789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963197-G-T

http://identifiers.org/hco/17/GRCh38#81198803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119963211-C-A

81198821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963223-G-C

81198946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119963305-G-A

81198946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119963305-G-C

81198946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119963305-G-T

81199116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963436-T-C

81199177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963480-G-A

81199238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963533-G-T

81199266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963562-G-C

81199266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119963562-G-T

http://identifiers.org/hco/17/GRCh38#81199381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119963664-C-A

81199381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119963664-C-T

81199616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119963871-G-A

81199616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119963871-G-T

81199744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119963979-C-G

81199744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119963979-C-T

81199755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119963990-C-T

http://identifiers.org/hco/17/GRCh38#81199897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119964132-C-A

81199897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119964132-C-G

81199897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119964132-C-T

81199919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119964158-T-C

http://identifiers.org/hco/17/GRCh38#81199969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119964189-C-A

81199969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119964189-C-T

81200134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119964353-A-G

81201166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119965614-G-A

81201224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119965691-G-A

81201293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119965763-G-C

81202293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119966443-C-G

81202293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119966443-C-T

81203697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119967095-G-A

81203697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119967095-G-T

81206595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119967636-T-C

81206893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119967898-G-C

81207042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119968055-G-A

81207042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119968055-G-T

81207085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119968110-T-A

81207085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119968110-T-C

81207130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119968158-C-T

81207224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119968252-T-C

81207315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119968331-A-G

81207333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119968353-G-T

http://identifiers.org/hco/17/GRCh38#81208796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119971936-C-A

81208823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119971962-G-A

81208823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119971962-G-T

81208872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972004-G-A

81208872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972004-G-T

81208902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972043-G-A

81208902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972043-G-T

81208907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972048-T-C

81208939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119972081-G-A

81208973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119972115-G-T

http://identifiers.org/hco/17/GRCh38#81209129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119972235-C-A

81209129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972235-C-T

81209168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972264-G-A

81209168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972264-G-C

81209168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972264-G-T

81209252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972327-G-A

81209252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972327-G-C

81209252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119972327-G-T

81219786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119974556-G-T

81219805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119974575-C-T

81219958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119974700-A-G

81219958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119974700-A-T

81219959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119974701-G-A

81219967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: synonymous variant
orthologous variants: 119974709-G-A

http://identifiers.org/hco/17/GRCh38#81220007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119974749-C-A

81220007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: missense variant
orthologous variants: 119974749-C-T

http://identifiers.org/hco/17/GRCh38#81220130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119974874-C-A

81220130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119974874-C-T

81220550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975269-A-G

81220625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975345-G-A

81220643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975361-C-T

81220843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975482-C-T

81220985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975635-C-T

http://identifiers.org/hco/17/GRCh38#81221041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119975690-C-A

81221094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975732-C-T

81221104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975742-A-G

http://identifiers.org/hco/17/GRCh38#81221106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119975744-C-A

81221106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975744-C-G

81221106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975744-C-T

81221172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975828-G-A

81221172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975828-G-C

81221195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119975851-T-A

81221415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119976169-C-T

81221596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119976459-C-T

81221655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119976558-T-G

81221813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119976835-G-A

81221884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119976905-C-G

81222058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119977050-G-A

81222058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: 119977050-G-T

http://identifiers.org/hco/17/GRCh38#81222245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119977240-C-A

http://identifiers.org/hco/17/GRCh38#81222639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119977438-C-A

81222639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 119977438-C-T

http://identifiers.org/hco/17/GRCh38#81222917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#119977580-C-A

81222917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119977580-C-T

81222929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5 prime UTR variant
orthologous variants: 119977592-A-G

81222929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5 prime UTR variant
orthologous variants: 119977592-A-T

http://identifiers.org/hco/17/GRCh38#81222955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119977619-C-A

81222955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5 prime UTR variant
orthologous variants: 119977619-C-T

81222980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29511
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119977644-C-T