92122008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 101942275-G-A

92122008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 101942275-G-C

92122008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 101942275-G-T

http://identifiers.org/hco/14/GRCh38#92122016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101942283-C-A

92122016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 101942283-C-T

http://identifiers.org/hco/14/GRCh38#92122157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#101942418-C-A

92122157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 101942418-C-T

92122248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 101942495-T-C

92122248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 101942495-T-G

http://identifiers.org/hco/14/GRCh38#92122354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101942598-A-C

92122354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942598-A-G

92122354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942598-A-T

92122376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942614-T-G

http://identifiers.org/hco/14/GRCh38#92122390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101942628-C-A

92122390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942628-C-T

http://identifiers.org/hco/14/GRCh38#92122393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101942630-C-A

92122393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942630-C-T

92122463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942694-C-G

http://identifiers.org/hco/14/GRCh38#92122492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101942724-C-A

92122492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942724-C-T

92122580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942790-C-G

92122680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101942870-A-G

92122824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943010-A-G

92123734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943165-T-G

92123815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943244-T-C

92123819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943247-G-A

92123895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943317-T-C

92124062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943460-G-A

92124092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943489-A-G

92124152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943538-G-C

92124167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943556-G-C

92124230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943603-T-C

92124262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943633-A-G

92124322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943693-C-G

92124503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943866-T-C

92124503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943866-T-G

92124547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101943909-A-G

92125005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101944307-G-A

92125133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101944641-G-A

92125154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101944663-G-A

92125281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101944790-A-G

92125287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101944796-C-G

92125287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101944796-C-T

92125523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101945019-A-G

92126046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101946427-T-C

92126140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 101947021-A-G

92126167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 101947045-C-T

92126262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101947125-G-T

92126292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101947151-C-T

92126439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101947311-T-A

http://identifiers.org/hco/14/GRCh38#92126458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101947330-A-C

92126458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101947330-A-G

92130116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101947517-A-G

92130293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101947675-T-G

92130781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948045-T-A

92130856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948098-G-T

92130946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 101948168-G-A

http://identifiers.org/hco/14/GRCh38#92131228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101948640-C-A

92131228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948640-C-T

92131248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948650-C-G

92131398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948807-G-A

92131407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948814-A-G

92131447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948852-G-A

92131870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101948952-G-A

92132023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949091-A-G

92132051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949117-C-T

92133128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949199-A-G

92133930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949357-G-A

http://identifiers.org/hco/14/GRCh38#92133959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101949386-C-A

92134080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 101949504-T-C

92134192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949616-A-T

92134270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 101949699-T-C

92134279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 101949708-C-G

92134279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 101949708-C-T

92134389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949951-G-T

92134430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101949996-G-T

92134528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101950077-T-C

http://identifiers.org/hco/14/GRCh38#92134554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101950103-A-C

92134620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101950146-A-G

92134638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101950164-T-G

92134874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101950920-G-C

92135216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951346-T-A

92135216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951346-T-C

92135216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951346-T-G

92135218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951348-A-T

92135287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951405-A-G

92135287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951405-A-T

92135295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 101951408-A-G

92135377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 101951490-T-C

http://identifiers.org/hco/14/GRCh38#92135530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101951643-C-A

92135568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101951678-A-G

http://identifiers.org/hco/14/GRCh38#92135571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101951681-A-C

92135571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101951681-A-G

92135606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101951720-A-G

92135633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101951747-T-C

92135990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101952074-C-T

92136144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101952221-A-G

92136182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101952269-G-A

92138198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101953485-T-C

92138362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101953646-A-G

92138362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101953646-A-T

http://identifiers.org/hco/14/GRCh38#92138366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101953650-C-A

92138376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101953676-A-G

92138428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101953732-A-G

92138428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101953732-A-T

92139905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101954225-G-T

http://identifiers.org/hco/14/GRCh38#92142012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101954763-C-A

92142012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101954763-C-G

92142067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101954797-A-G

92142067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101954797-A-T

92142093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101954821-A-G

92142315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: synonymous variant
orthologous variants: 101955043-T-C

92142327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: synonymous variant
orthologous variants: 101955055-T-C

92142830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101955889-G-A

92142837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101955896-T-C

http://identifiers.org/hco/14/GRCh38#92142882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101955938-C-A

92142925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101955975-G-C

92142925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101955975-G-T

92142978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101956021-T-A

92143311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101956355-G-T

92144502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101957750-A-T

92144692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101957910-T-C

http://identifiers.org/hco/14/GRCh38#92144732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101957946-C-A

92144919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958063-A-G

92145268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958273-C-T

92145382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958298-G-C

92145392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958308-T-C

92145463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: -A-T

92145478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958387-C-T

92145491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958399-A-G

92145563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958471-G-A

92145563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958471-G-C

92145819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101958724-C-T

92146814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101959825-A-G

92147169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101960113-T-C

92147516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101960605-A-G

92154211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101962970-G-A

92154211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101962970-G-T

http://identifiers.org/hco/14/GRCh38#92154307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101963039-C-A

92154307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101963039-C-T

92154476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963201-A-G

http://identifiers.org/hco/14/GRCh38#92154516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101963253-C-A

92154536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963273-G-A

92154536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963273-G-T

92154580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963316-A-G

92154594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963330-T-C

92154596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963332-G-C

92155067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963464-T-A

92155067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963464-T-C

92155144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101963535-T-C

92155344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101963735-T-C

92155421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101963762-T-A

92155432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101963770-A-G

92155516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101963856-C-T

92155606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101963945-A-G

92156201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101964521-A-G

92156447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101964765-T-G

92156710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965025-T-A

92156736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965053-A-G

92156737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965054-G-T

92156744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965061-T-G

92156924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965225-C-T

92156940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965243-G-A

92156954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965257-T-C

92156975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965278-T-A

http://identifiers.org/hco/14/GRCh38#92157220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101965483-A-C

92157621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965594-T-G

92157629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965602-G-A

http://identifiers.org/hco/14/GRCh38#92157734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101965707-A-C

92157803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: synonymous variant
orthologous variants: 101965776-C-T

92157942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965904-G-A

92157942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965904-G-T

92157995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965946-T-G

92158009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965960-T-A

92158009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965960-T-C

92158023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101965974-G-A

http://identifiers.org/hco/14/GRCh38#92158024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101965975-C-A

92158047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966004-A-G

92158204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966158-G-T

92158209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966163-G-C

92158209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966163-G-T

92158211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966165-G-A

92158211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966165-G-C

92158235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966194-G-A

http://identifiers.org/hco/14/GRCh38#92158869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101966838-A-C

92158869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101966838-A-G

http://identifiers.org/hco/14/GRCh38#92158943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101966910-C-A

92159258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: synonymous variant
orthologous variants: 101967211-T-G

92159865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101967547-G-T

92160712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, undefined
orthologous variants: 101968501-A-G

92160886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron_variant, undefined
orthologous variants: 101968667-G-T

http://identifiers.org/hco/14/GRCh38#92161005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101968783-A-C

92161005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101968783-A-G

92161026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101968803-A-G

92161147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: synonymous variant
orthologous variants: 101968922-A-G

92161213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: synonymous variant
orthologous variants: 101968988-A-T

92161266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101969041-G-A

92161272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101969047-A-G

http://identifiers.org/hco/14/GRCh38#92161365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101969129-A-C

92161512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101969250-A-G

92161599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101969335-G-A

92161599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: intron variant
orthologous variants: 101969335-G-T

92161781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101969518-T-A

92161986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101969808-G-A

http://identifiers.org/hco/14/GRCh38#92162084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101969934-C-A

92162084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101969934-C-T

http://identifiers.org/hco/14/GRCh38#92162106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101969956-A-C

92162374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101970179-A-G

http://identifiers.org/hco/14/GRCh38#92162473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101970395-C-A

92162490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101970416-T-A

92162534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101970463-G-A

92162626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101970552-G-T

http://identifiers.org/hco/14/GRCh38#92162905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101970794-C-A

92162905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101970794-C-G

http://identifiers.org/hco/14/GRCh38#92162906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101970795-C-A

http://identifiers.org/hco/14/GRCh38#92163161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101970827-C-A

92163517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971132-A-G

92164295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971215-A-G

http://identifiers.org/hco/14/GRCh38#92164331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971251-C-A

92164358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971277-G-A

http://identifiers.org/hco/14/GRCh38#92164440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971359-A-C

http://identifiers.org/hco/14/GRCh38#92164481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971401-C-A

92164533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971450-G-A

92164533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971450-G-T

92164534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971451-A-G

92164536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971453-G-A

92164545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971462-A-G

http://identifiers.org/hco/14/GRCh38#92164549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971468-C-A

92164583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971503-G-T

92164602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971517-G-A

92164602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971517-G-T

92164703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971749-C-G

http://identifiers.org/hco/14/GRCh38#92164766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971836-A-C

http://identifiers.org/hco/14/GRCh38#92164780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971850-C-A

92164793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971863-A-G

92164824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971896-A-G

92164837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971910-T-C

http://identifiers.org/hco/14/GRCh38#92164887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101971949-C-A

92164887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971949-C-G

92164887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101971949-C-T

http://identifiers.org/hco/14/GRCh38#92164974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101972043-C-A

92164974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972043-C-G

92164974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972043-C-T

http://identifiers.org/hco/14/GRCh38#92165025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101972076-C-A

92165094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972253-A-G

http://identifiers.org/hco/14/GRCh38#92165195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101972342-C-A

92165195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972342-C-G

92165335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972490-C-G

http://identifiers.org/hco/14/GRCh38#92165389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101972539-C-A

92165389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972539-C-T

http://identifiers.org/hco/14/GRCh38#92165470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101972613-A-C

92165489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972634-C-T

92165530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972679-T-C

92165595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972771-C-T

92165596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972772-T-C

92165709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101972924-A-G

http://identifiers.org/hco/14/GRCh38#92167307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101973658-C-A

92167307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101973658-C-G

92167372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101973715-G-A

92167510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101973851-G-T

92170792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101975328-A-G

92171540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976020-T-C

92171563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976043-A-G

92171613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976087-A-G

92171641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976111-G-A

92171641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976111-G-T

92171696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976168-G-T

92171710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976190-C-T

http://identifiers.org/hco/14/GRCh38#92171758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101976225-C-A

92171760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976227-C-T

92171923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976317-G-T

92171936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976330-G-A

92171936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976330-G-T

92171976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976342-T-C

http://identifiers.org/hco/14/GRCh38#92172095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#101976453-C-A

92172121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2325
most severe consequence: 3 prime UTR variant
orthologous variants: 101976477-G-T