45534654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75941556-A-G

45534667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75941543-G-T

45534687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75941513-A-G

45534687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75941513-A-T

45534799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941404-G-A

45534799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941404-G-T

45534817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941386-G-A

45534817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941386-G-T

45534825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941378-G-A

45534825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941378-G-C

45534825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941378-G-T

45534835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941368-G-A

45534835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75941368-G-T

45534952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75941292-G-T

45535009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75941235-A-G

45535411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940886-A-G

45535441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940861-T-C

45535464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940838-G-T

http://identifiers.org/hco/13/GRCh38#45535493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75940809-C-A

45535495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940807-A-G

http://identifiers.org/hco/13/GRCh38#45535510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75940793-A-C

45535510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940793-A-G

45535532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940771-G-A

45535532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940771-G-C

45535532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940771-G-T

45535557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940748-C-T

45535683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940670-T-C

45535706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940646-G-T

45535743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940624-A-G

45535746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940621-C-T

45535797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940572-T-C

http://identifiers.org/hco/13/GRCh38#45535821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75940548-C-A

45535821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940548-C-T

45535849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940515-G-A

http://identifiers.org/hco/13/GRCh38#45535865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75940493-C-A

45535865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940493-C-G

45535865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940493-C-T

45535944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940425-G-A

45535944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940425-G-T

45536347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75940054-C-T

45536429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75939987-C-G

45536459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75939957-C-T

45536513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75939903-A-T

45536653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75939760-G-A

45536653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75939760-G-T

http://identifiers.org/hco/13/GRCh38#45536748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75939680-C-A

http://identifiers.org/hco/13/GRCh38#45536763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75939666-C-A

45536786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75939644-A-G

http://identifiers.org/hco/13/GRCh38#45536857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75939580-A-C

45537277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75937290-A-G

45537406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75937188-A-G

45537407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75937187-G-A

45537436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75937160-T-C

45537576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75937034-T-A

45538611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935918-C-T

45539537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935648-C-T

45539808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935404-C-T

http://identifiers.org/hco/13/GRCh38#45539817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75935395-C-A

45539817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935395-C-T

45539896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935324-A-G

45540087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935165-C-T

45540147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75935101-C-T

45540449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934902-T-A

45541055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934469-G-A

45541074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934450-A-T

45541154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934372-A-T

http://identifiers.org/hco/13/GRCh38#45541165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75934361-C-A

http://identifiers.org/hco/13/GRCh38#45541173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75934352-C-A

45541173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934352-C-T

45541174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934351-T-C

45541187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934334-G-A

45541187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934334-G-C

45541197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75934324-G-C

45541537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75934002-G-A

45541537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75934002-G-C

45541729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75933812-C-G

45541729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75933812-C-T

http://identifiers.org/hco/13/GRCh38#45541762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75933779-C-A

45541762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75933779-C-T

http://identifiers.org/hco/13/GRCh38#45541763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75933778-C-A

45541763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75933778-C-T

45541807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75933735-G-T

45541857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75933686-C-T

45544830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75931608-T-C

45544902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75931536-T-A

45544995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75931445-G-A

45544995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75931445-G-C

45545091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75931322-G-T

45548824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75930051-G-A

http://identifiers.org/hco/13/GRCh38#45548825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75930050-C-A

45548877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75930000-C-G

http://identifiers.org/hco/13/GRCh38#45549755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75929530-C-A

45549788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929496-G-A

45549788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929496-G-T

45549821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929474-G-A

45549838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929462-T-A

45549873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929438-G-A

45549873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929438-G-T

45550101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929206-G-A

http://identifiers.org/hco/13/GRCh38#45550141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75929166-C-A

45550141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929166-C-T

45550144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75929163-A-G

45550230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 75929135-C-G

45550309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75929056-T-C

45550320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75929045-G-A

45550390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75928977-T-C

http://identifiers.org/hco/13/GRCh38#45550442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75928931-C-A

45550442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75928931-C-T

http://identifiers.org/hco/13/GRCh38#45550780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75928444-C-A

45550974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75928258-G-T

45551369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75927927-T-C

http://identifiers.org/hco/13/GRCh38#45551427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75927871-C-A

45561153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924564-G-C

45561229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924489-T-A

45561229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924489-T-C

http://identifiers.org/hco/13/GRCh38#45561231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75924487-C-A

45561231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924487-C-T

45561353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924357-G-A

45561470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense variant
orthologous variants: 75924245-G-A

45561583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924120-A-G

45561583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924120-A-T

45561606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924094-G-A

45561606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924094-G-T

45561631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924070-G-T

45561639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924062-G-A

45561639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75924062-G-T

45561753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75923966-A-G

45561838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75923876-G-A

http://identifiers.org/hco/13/GRCh38#45561981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75923737-A-C

45562041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75923293-T-G

45562112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75923219-G-C

45562413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron variant
orthologous variants: 75922841-A-G

45563702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75921126-T-C

http://identifiers.org/hco/13/GRCh38#45563794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75921034-A-C

45563795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75921033-G-A

45563817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75921011-G-A

http://identifiers.org/hco/13/GRCh38#45563831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75920998-C-A

45563831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920998-C-G

45563857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920972-G-A

45563857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920972-G-T

45564049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920780-G-A

45568094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920325-C-T

http://identifiers.org/hco/13/GRCh38#45568193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75920243-A-C

45568193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920243-A-G

45568202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920234-G-C

45568202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920234-G-T

45568215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920221-T-C

45568247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920188-T-C

http://identifiers.org/hco/13/GRCh38#45568272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75920164-C-A

45568272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920164-C-T

http://identifiers.org/hco/13/GRCh38#45568280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75920156-C-A

45568379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75920061-C-T

45568393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75920047-T-C

45568883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75918370-A-G

45569009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75918254-G-C

http://identifiers.org/hco/13/GRCh38#45569447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75918181-C-A

45569475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75918150-T-C

45569607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75918017-A-G

45569729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75917882-A-G

45569881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75917742-C-T

45570506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75917400-T-C

http://identifiers.org/hco/13/GRCh38#45570539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75917373-C-A

45570539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75917373-C-T

45570606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75917306-G-A

45570631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75917294-G-A

45572589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75915257-T-C

http://identifiers.org/hco/13/GRCh38#45572662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75915184-C-A

45572842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75914845-A-G

45573169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75914451-A-G

45573211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75914412-A-G

45573380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75914243-C-T

45575257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75913436-C-T

45575258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75913435-C-T

45575533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75913231-G-A

45575533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75913231-G-T

45575632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75913133-G-A

45575632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75913133-G-T

45575844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912933-C-T

45576089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912691-T-G

45576160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912650-C-T

45576215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912628-G-T

45576355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912507-C-T

45576581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912309-G-A

45576776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75912109-A-G

45576900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75911978-T-C

45577072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75911828-G-A

45577115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75911787-T-C

45577125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75911783-C-G

45577126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75911782-C-T

45578057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75910867-G-A

45578100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75910824-A-T

http://identifiers.org/hco/13/GRCh38#45578115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75910809-A-C

45578335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75910619-T-C

45578403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75910541-C-T

45578724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75910267-C-G

45579212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75910024-G-A

45579330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909914-C-T

http://identifiers.org/hco/13/GRCh38#45579347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75909901-C-A

45579593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909678-A-G

45579593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909678-A-T

45579784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909486-G-A

45579784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909486-G-T

http://identifiers.org/hco/13/GRCh38#45579789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75909481-C-A

45579789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909481-C-T

45579830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909440-T-A

45579832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909438-A-G

45579837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909433-G-A

45579837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909433-G-C

45579837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909433-G-T

45579872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909399-C-T

45579882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909389-G-A

45580010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909302-G-A

45580010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909302-G-T

45580099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909232-T-G

http://identifiers.org/hco/13/GRCh38#45580102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75909229-C-A

45580102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909229-C-G

45580138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909186-C-G

http://identifiers.org/hco/13/GRCh38#45580381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75909011-C-A

45580381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75909011-C-T

45580557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75908864-G-A

45580557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75908864-G-T

45580594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75908836-A-G

45580813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75908626-G-A

45580828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75908610-C-T

http://identifiers.org/hco/13/GRCh38#45580829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75908609-C-A

http://identifiers.org/hco/13/GRCh38#45580903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75908567-C-A

http://identifiers.org/hco/13/GRCh38#45581055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75908472-C-A

http://identifiers.org/hco/13/GRCh38#45581057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75908470-C-A

45581368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75908173-C-T

http://identifiers.org/hco/13/GRCh38#45582789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75907417-C-A

45583046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75907181-G-A

http://identifiers.org/hco/13/GRCh38#45583118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75907112-C-A

45583160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75907071-G-A

45583160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75907071-G-C

45583227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75907007-T-C

45583273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75906967-C-T

45584049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75906160-A-G

45584227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905989-G-A

45584605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905647-G-A

45584732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905545-T-C

45584737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905540-G-A

45584832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905418-C-T

45584842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905410-C-T

45584853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905399-A-G

45584887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905365-T-G

45584940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905318-C-T

45585081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905194-C-G

45585081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905194-C-T

45585134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75905135-T-A

45585363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75904950-G-C

45585364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75904949-C-T

45585411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75904913-T-C

http://identifiers.org/hco/13/GRCh38#45585589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75904175-A-C

http://identifiers.org/hco/13/GRCh38#45585707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75904055-C-A

45585707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75904055-C-T

45585764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903984-C-T

http://identifiers.org/hco/13/GRCh38#45585783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75903965-C-A

45585983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903782-A-G

45586116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903657-C-T

45586157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903636-T-C

45586191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903602-C-T

45586211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903581-C-T

45586410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903383-T-C

45586758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75903055-C-T

45586944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902884-G-T

45587048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902738-C-G

45587048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902738-C-T

http://identifiers.org/hco/13/GRCh38#45587205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75902584-C-A

45587205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75902584-C-T

45587218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75902571-C-T

45587238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75902551-A-G

45587249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902540-C-G

45587249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902540-C-T

45587315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902467-G-A

45587315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902467-G-C

45587315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902467-G-T

45587321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902461-C-T

45587336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902429-C-T

45587381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75902382-C-T

45589903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75901934-G-A

45589903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75901934-G-T

45590271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75901417-T-C

http://identifiers.org/hco/13/GRCh38#45590291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75901396-C-A

45590291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75901396-C-T

http://identifiers.org/hco/13/GRCh38#45590558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75901109-C-A

45590558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75901109-C-T

45590726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900978-A-G

45590726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900978-A-T

45590783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900908-G-C

45590783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900908-G-T

45590795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900897-T-C

45590801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900891-T-A

45590801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900891-T-G

http://identifiers.org/hco/13/GRCh38#45590833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75900809-C-A

45590833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900809-C-T

45591009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900593-G-A

45591091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75900507-T-C

45593890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899696-T-C

45593944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899641-A-G

45594224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899352-T-C

45594256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899320-G-A

45594414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75899151-C-T

45594977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75898691-G-A

http://identifiers.org/hco/13/GRCh38#45596186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75896970-C-A

45596186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896970-C-T

45596191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896965-T-C

45596213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896946-T-G

http://identifiers.org/hco/13/GRCh38#45596265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75896904-C-A

45596265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896904-C-T

45596307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896865-A-G

45596325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896846-A-G

45596332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896843-T-C

45596345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896830-G-A

45596345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896830-G-T

45596360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75896818-G-T

http://identifiers.org/hco/13/GRCh38#45596369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#75896806-C-A

45596369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75896806-C-T

45596391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896787-A-G

45596436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896734-C-T

http://identifiers.org/hco/13/GRCh38#45596441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#75896729-C-A

45596441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75896729-C-T

45596481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896679-A-G

45596493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896667-C-T

45596522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75896628-C-T

45596526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896624-C-T

45596547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896593-C-T

45596562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896578-C-T

45596625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896495-G-A

45596634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75896486-C-G

45596634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896486-C-T

45596652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896459-C-T

45596661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896449-A-G

http://identifiers.org/hco/13/GRCh38#45596666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#75896444-C-A

45596666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75896444-C-T

http://identifiers.org/hco/13/GRCh38#45596706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75896395-C-A

45596706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75896395-C-T

45596910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-G

45596924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75896192-G-A

45596924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75896192-G-T

45597189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895933-T-A

45597189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895933-T-C

http://identifiers.org/hco/13/GRCh38#45597212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75895904-C-A

45597212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895904-C-T

45597329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895810-A-G

45597551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895610-T-C

45597561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895600-A-G

45597762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895405-T-A

45597763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75895404-T-A

45601111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75893899-G-C

45601300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75893782-C-G

45601414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75893759-C-G

45606467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889249-T-G

45606472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889244-T-A

http://identifiers.org/hco/13/GRCh38#45606483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75889237-C-A

http://identifiers.org/hco/13/GRCh38#45606490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75889231-C-A

45606625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889167-C-T

45606751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889102-A-G

45606753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889100-C-T

45606758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75889096-T-C

45607211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888746-A-G

45607461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888497-G-A

45607461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888497-G-T

45607471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888492-G-T

45607509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888454-A-G

45607529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888434-A-T

http://identifiers.org/hco/13/GRCh38#45607598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75888366-A-C

45607675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75888289-T-C

45611119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885330-T-C

45611188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885256-G-A

45611270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885178-C-G

45611270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885178-C-T

45611290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75885158-G-A

45611730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884744-G-A

45611868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75884619-C-T

45612694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75883783-T-C

http://identifiers.org/hco/13/GRCh38#45613174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75883070-C-A

45613469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75882825-G-A

45613819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881853-T-C

45613831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881847-T-A

http://identifiers.org/hco/13/GRCh38#45613944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75881759-A-C

45614030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881690-C-T

45614067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75881655-G-A

45614730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880616-T-G

45614741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880605-T-A

45614836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880520-G-A

45614837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880519-A-G

45614837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880519-A-T

45614862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880495-T-A

45614862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880495-T-C

45614933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880445-A-T

http://identifiers.org/hco/13/GRCh38#45614951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75880425-C-A

45615139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75880209-T-C

45615424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879972-G-A

45615435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879957-G-A

http://identifiers.org/hco/13/GRCh38#45615454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75879938-A-C

45615454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879938-A-G

45615642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879769-G-A

45615642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75879769-G-T

45615703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26523
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75879708-C-T