http://identifiers.org/hco/22/GRCh38#45502751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090132-C-A

45502751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85090132-C-T

45502800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85090180-G-A

45502870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090244-G-A

45502870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090244-G-T

http://identifiers.org/hco/22/GRCh38#45502873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090247-C-A

45502873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090247-C-G

45502885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090259-T-C

45502887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090261-G-A

45502887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090261-G-T

http://identifiers.org/hco/22/GRCh38#45502941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090299-C-A

45502941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090299-C-T

45502968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090326-G-A

45502968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090326-G-C

45502968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85090326-G-T

http://identifiers.org/hco/22/GRCh38#45503002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090351-C-A

45503002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, missense_variant
orthologous variants: 85090351-C-G

45503002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, missense_variant
orthologous variants: 85090351-C-T

45503057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090406-G-A

45503057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090406-G-T

http://identifiers.org/hco/22/GRCh38#45503113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090458-C-A

45503113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090458-C-G

45503113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090458-C-T

http://identifiers.org/hco/22/GRCh38#45503121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090466-C-A

45503121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090466-C-G

45503121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090466-C-T

http://identifiers.org/hco/22/GRCh38#45503141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090486-A-C

45503141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090486-A-G

http://identifiers.org/hco/22/GRCh38#45503207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090556-C-A

45503207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090556-C-G

45503207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090556-C-T

http://identifiers.org/hco/22/GRCh38#45503213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090562-C-A

45503213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090562-C-T

http://identifiers.org/hco/22/GRCh38#45503217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090566-C-A

45503217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090566-C-T

http://identifiers.org/hco/22/GRCh38#45503222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090571-C-A

45503222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090571-C-G

45503222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090571-C-T

45503252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090604-T-A

45503252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090604-T-C

45503252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85090604-T-G

http://identifiers.org/hco/22/GRCh38#45503256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090608-C-A

45503256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090608-C-G

45503256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090608-C-T

45503263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090615-G-A

http://identifiers.org/hco/22/GRCh38#45503299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090644-A-C

45503299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85090644-A-G

45503352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85090676-T-C

45503375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85090697-G-A

45503375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85090697-G-T

45503441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85090736-G-A

45503441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85090736-G-T

http://identifiers.org/hco/22/GRCh38#45503449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85090744-C-A

45503580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85090862-G-T

45503826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85090970-C-T

45503878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85091020-G-A

45504218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-G

45504443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85091533-A-T

45504617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85091678-C-T

45504664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85091708-G-A

45505569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85092501-G-A

45507135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85094064-G-A

45507270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85094182-T-G

45507456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85094367-T-A

45508857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095014-G-C

45508866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095024-T-G

45508985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095131-T-G

45509121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095224-C-T

45509283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095376-C-T

45509323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095415-G-A

45509323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095415-G-T

45509375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85095463-C-T

45510678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85096138-T-C

45510689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85096149-A-G

45512320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85099048-C-G

45512563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85099245-A-G

45513037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85099937-G-A

45513114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85100013-C-G

45513148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85100034-T-C

45513170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85100056-C-T

45513209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85100096-T-C

45513220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85100107-A-G

45514123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101514-C-T

45514316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101665-G-T

http://identifiers.org/hco/22/GRCh38#45514405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85101774-A-C

45514436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101808-A-G

45514455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101826-C-T

45514498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101839-C-G

45514509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101850-G-A

45514518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101859-C-G

45514570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101909-T-C

45514598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85101937-C-T

45514730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85102061-G-A

45514730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85102061-G-C

45514864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85102127-C-T

45514870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85102133-C-T

45514934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85102176-C-G

45515318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85103114-C-T

45515398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85103223-A-G

45515460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85103297-G-A

45515462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85103299-G-A

http://identifiers.org/hco/22/GRCh38#45515629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85103428-C-A

45515682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85103473-A-G

45516320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85104100-C-T

45516647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85104494-G-T

45516737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85104579-G-T

45516887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85104725-C-G

45517294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85105291-G-A

45517294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85105291-G-T

45517501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85105453-G-A

45517501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85105453-G-T

45517720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105596-T-A

45518399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105828-C-G

45518462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105883-A-G

45518462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105883-A-T

45518488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105906-G-T

45518497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105915-G-A

45518497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105915-G-T

45518501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105919-A-G

http://identifiers.org/hco/22/GRCh38#45518550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85105967-C-A

45518550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105967-C-G

45518550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85105967-C-T

45518612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85106044-G-A

45518612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85106044-G-T

45518646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85106069-T-G

45518761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85106184-A-G

45518834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106254-G-A

45518834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106254-G-C

45518842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106262-T-A

45518842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106262-T-C

45518844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106264-G-A

45518878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106292-G-A

45518878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106292-G-C

45519008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106385-C-T

45519026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106403-C-T

45519313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85106684-G-A

45524023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107645-C-T

45524090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107710-T-C

45524251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107825-G-A

45524349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107917-C-T

45524361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107929-C-G

45524382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107948-G-A

45524382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85107948-G-T

45524436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108005-C-T

45524462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108038-A-G

45524543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108120-A-G

45524667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108212-A-G

45524742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108263-G-A

45524757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108278-C-T

45525409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108334-G-A

45525409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108334-G-T

45525453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108376-T-C

45525473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108394-A-T

45525481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108402-G-A

45525481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108402-G-C

45525481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108402-G-T

http://identifiers.org/hco/22/GRCh38#45525632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85108540-C-A

45525632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense variant
orthologous variants: 85108540-C-T

45525866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108670-C-T

45525912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108706-G-A

45525912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108706-G-C

45525912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108706-G-T

45525999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108798-C-T

45526000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85108799-T-C

45526328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85109114-G-A

45526373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85109153-C-T

45526400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85109179-T-G

45526763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85109875-G-C

45526860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85109954-G-A

http://identifiers.org/hco/22/GRCh38#45527011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85110108-C-A

45527011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85110108-C-G

45527089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85110180-C-T

45527749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85111058-G-C

45527749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85111058-G-T

45527870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85111192-G-A

45527906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85111228-G-A

45527906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 85111228-G-C

45528041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85111373-G-A

45531308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85113801-G-A

45531370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85113868-A-G

http://identifiers.org/hco/22/GRCh38#45532017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85114202-A-C

45532017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85114202-A-G

45532056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85114237-A-G

45532152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85114332-A-G

45532361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85114508-C-T

45532521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114570-A-G

45532630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114637-G-T

45532653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114661-G-A

http://identifiers.org/hco/22/GRCh38#45532746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85114746-C-A

45532746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114746-C-T

45532780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114777-T-A

45532780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114777-T-C

http://identifiers.org/hco/22/GRCh38#45532871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85114850-C-A

45532871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114850-C-G

45532871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114850-C-T

45532877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114854-G-A

45532877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114854-G-C

45532877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114854-G-T

45532885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85114862-C-T

45532893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85114870-A-T

45532943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85114915-G-A

45532943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85114915-G-C

45532943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85114915-G-T

45532962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85114933-T-A

45533103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85115040-C-T

45533468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115329-C-G

45533468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115329-C-T

45533622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115467-G-A

45533765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85115622-C-T

45533987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115844-G-A

45533987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115844-G-T

45534200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115969-G-T

45534204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115976-G-A

45534226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115994-G-T

45534229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85115997-C-T

http://identifiers.org/hco/22/GRCh38#45534275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85116031-C-A

http://identifiers.org/hco/22/GRCh38#45534285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85116041-C-A

45534285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85116041-C-T

http://identifiers.org/hco/22/GRCh38#45534327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85116052-A-C

45535385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85116918-G-A

45535509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85116990-G-A

45535509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85116990-G-T

45535530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85117015-T-A

45535530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85117015-T-C

45535548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85117025-T-A

45535548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85117025-T-C

45535554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85117031-A-T

45535594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117066-G-A

45535594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117066-G-C

45535669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117146-G-A

45535669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117146-G-T

45535747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117239-A-G

45535773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117265-G-A

45535863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117360-G-A

45537666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117887-A-G

45537782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117971-C-T

45537783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85117972-G-A

45537909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85118089-G-A

45537909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85118089-G-C

45537909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85118089-G-T

45537942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85118110-T-C

http://identifiers.org/hco/22/GRCh38#45538208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85118375-C-A

45540615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121172-T-A

45540747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121296-C-T

45540878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121489-G-A

45540932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121563-G-A

45541086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121666-G-A

45541086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121666-G-T

45541102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121682-G-T

45541104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121684-G-A

45541104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121684-G-C

45541104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121684-G-T

45541121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121702-G-C

45541121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121702-G-T

45541173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121752-G-A

45541174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85121753-G-A

45541387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122015-A-G

45541389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122017-C-T

45541539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122170-C-T

45541692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122298-A-G

http://identifiers.org/hco/22/GRCh38#45541719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85122312-A-C

45541719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122312-A-G

45541872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122450-G-A

45541872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122450-G-T

45542094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122610-T-C

45542135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85122644-C-T

45542149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85122658-T-C

45542149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85122658-T-G

45542180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 85122689-T-G

45542234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85122743-C-T

45542280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85122789-G-A

45542323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122829-A-G

45542330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122836-A-T

45542347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122856-G-A

45542347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122856-G-C

45542347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122856-G-T

45542350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122859-G-T

45542364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122874-G-A

45542364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122874-G-T

45542367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122880-G-A

45542367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122880-G-T

http://identifiers.org/hco/22/GRCh38#45542375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85122888-C-A

http://identifiers.org/hco/22/GRCh38#45542406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85122919-C-A

45542406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122919-C-T

45542450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85122962-G-A

45542819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123286-G-C

45543308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123406-G-A

45543308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123406-G-T

45543352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123447-T-C

45543353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123448-G-A

45543353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123448-G-T

http://identifiers.org/hco/22/GRCh38#45543355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85123450-C-A

45543355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123450-C-G

45543365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123460-G-A

45543365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123460-G-T

45543388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85123482-C-T

45543426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85123520-C-G

45543426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85123520-C-T

http://identifiers.org/hco/22/GRCh38#45543474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85123568-C-A

45543474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85123568-C-T

45545706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85124075-G-A

45546910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85124648-G-A

http://identifiers.org/hco/22/GRCh38#45546957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85124682-C-A

45546957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85124682-C-T

45547062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85124801-G-A

45547067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85124806-C-G

45547067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85124806-C-T

45547125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85124861-T-C

45547212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85124948-C-T

http://identifiers.org/hco/22/GRCh38#45547302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85125014-C-A

45547302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85125014-C-G

45547310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85125022-A-T

45547323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85125035-A-G

45547323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85125035-A-T

http://identifiers.org/hco/22/GRCh38#45547324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85125036-C-A

45547324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85125036-C-T

45547372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85125082-T-C

45548519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126111-G-A

45548519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126111-G-C

45548519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126111-G-T

45548529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126120-G-T

45548532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126123-G-A

45548532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126123-G-C

45548590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126188-T-C

45548603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126202-G-C

45548846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126430-G-T

45549021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126541-C-T

45549032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126552-C-T

45549124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126708-G-A

45549266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85126867-C-G

45549428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85127016-G-A

45549494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85127348-G-A

45549518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85127374-G-A

45549518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85127374-G-C

45549518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85127374-G-T

45549988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85127950-C-T

http://identifiers.org/hco/22/GRCh38#45550391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128269-C-A

45550406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128282-A-G

45550406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128282-A-T

http://identifiers.org/hco/22/GRCh38#45550420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128313-C-A

45550420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128313-C-G

45550420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128313-C-T

45550427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128320-G-A

45550427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128320-G-T

45550437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128330-G-A

45550441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128334-A-G

45550458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128351-T-C

45550463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128356-T-C

http://identifiers.org/hco/22/GRCh38#45550520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128412-C-A

45550520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85128412-C-T

45550535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85128427-C-G

45550535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85128427-C-T

http://identifiers.org/hco/22/GRCh38#45550562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128454-C-A

45550562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85128454-C-T

45550669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128557-A-T

45550685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128578-G-T

45550698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128591-G-A

45550698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128591-G-T

http://identifiers.org/hco/22/GRCh38#45550730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128618-C-A

45550730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128618-C-G

45550730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128618-C-T

http://identifiers.org/hco/22/GRCh38#45550736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128624-A-C

45550772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128652-T-A

http://identifiers.org/hco/22/GRCh38#45550785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128665-C-A

45550785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128665-C-T

45550815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128692-G-A

45550815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85128692-G-T

http://identifiers.org/hco/22/GRCh38#45550839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128715-C-A

45550934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85128740-G-T

http://identifiers.org/hco/22/GRCh38#45550950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128756-C-A

http://identifiers.org/hco/22/GRCh38#45550966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128770-C-A

45550966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85128770-C-T

45551026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85128834-C-T

http://identifiers.org/hco/22/GRCh38#45551062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128858-C-A

45551062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85128858-C-T

http://identifiers.org/hco/22/GRCh38#45551164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85128939-C-A

45551249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129028-T-C

45551312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129079-T-C

45551438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129209-G-T

45551702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129593-T-A

45551702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129593-T-C

45551702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129593-T-G

45551971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129819-T-C

45551974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129822-G-A

45551974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129822-G-C

45551995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85129843-C-G

45552202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85130017-A-G

45552202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85130017-A-T

45552374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85130175-A-G

45552388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85130192-C-T

45552467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85131278-C-G

45552851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132182-C-T

45552917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132238-T-G

45553005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132323-C-T

45553112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132371-C-T

45553141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132387-C-T

45553182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132418-C-T

45553321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132536-C-G

45553321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132536-C-T

45553357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132546-A-T

45553371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85132560-C-G

45554235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, undefined
orthologous variants: 85134017-C-G

45554316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, undefined
orthologous variants: 85134080-C-T

45554325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, undefined
orthologous variants: 85134091-G-C

45554354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134119-C-T

45554363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134128-T-G

45554366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134131-A-T

45554568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134366-G-C

45554731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134520-C-G

45554793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134590-A-G

45554836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85134630-G-A

45562277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135072-G-T

45562300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135093-G-T

http://identifiers.org/hco/22/GRCh38#45562446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85135213-C-A

45562483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135249-C-T

45562553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135299-G-A

http://identifiers.org/hco/22/GRCh38#45562557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85135303-C-A

45562748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135461-G-A

http://identifiers.org/hco/22/GRCh38#45562830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85135564-C-A

45562830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135564-C-G

45562830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135564-C-T

45562864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135598-G-T

45562891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85135625-C-T

45563283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85136016-G-A

45563283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85136016-G-C

http://identifiers.org/hco/22/GRCh38#45563374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85136099-C-A

45563374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136099-C-T

http://identifiers.org/hco/22/GRCh38#45563416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85136144-A-C

http://identifiers.org/hco/22/GRCh38#45563419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85136147-C-A

45563419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136147-C-T

http://identifiers.org/hco/22/GRCh38#45563436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85136164-C-A

45563436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136164-C-T

45563486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136212-A-G

45563486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136212-A-T

45563506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136232-T-A

45563510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136236-T-C

45563948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85136613-C-T

45573994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85146976-T-C

http://identifiers.org/hco/22/GRCh38#45574051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85147030-A-C

45574051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147030-A-G

45574203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147210-T-G

45574256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147259-G-T

http://identifiers.org/hco/22/GRCh38#45574356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85147333-C-A

http://identifiers.org/hco/22/GRCh38#45574398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85147375-C-A

45574398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147375-C-G

45574398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147375-C-T

45574483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147431-C-G

45574497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147446-G-A

45574511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 85147460-G-T

45574516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense variant
orthologous variants: 85147465-A-G

45574532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense variant
orthologous variants: 85147481-C-G

http://identifiers.org/hco/22/GRCh38#45574577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#85147526-C-A

45574577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: synonymous variant
orthologous variants: 85147526-C-T

45574611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense variant
orthologous variants: 85147560-G-A

45574671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147619-G-A

45574671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147619-G-C

45574671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147619-G-T

http://identifiers.org/hco/22/GRCh38#45574701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85147651-C-A

45574701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147651-C-G

45574701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147651-C-T

http://identifiers.org/hco/22/GRCh38#45574754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85147704-C-A

45575176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147767-T-C

45575379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147946-G-T

45575382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147949-G-A

45575382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147949-G-C

45575382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147949-G-T

45575389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85147956-T-C

45575467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148002-A-G

45575528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148054-T-C

45576042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148487-G-A

45576042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148487-G-C

45576042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148487-G-T

45576050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148495-G-T

45576283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148852-A-G

45576312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85148899-G-A

45576766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149208-C-T

http://identifiers.org/hco/22/GRCh38#45576835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85149274-A-C

45576895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149333-A-G

45576941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149394-C-T

45576945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149398-G-A

45576946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149399-C-T

45576948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149401-G-T

45577014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: synonymous variant
orthologous variants: 85149488-T-C

45577092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: missense variant
orthologous variants: 85149566-G-A

http://identifiers.org/hco/22/GRCh38#45577156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85149614-A-C

45577156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149614-A-G

http://identifiers.org/hco/22/GRCh38#45577157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85149615-C-A

45577157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149615-C-T

45577300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149728-C-T

45577305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149733-T-A

45577428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85149851-T-C

45577640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85150046-G-A

45577973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 85150931-C-T

45577986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, missense_variant
orthologous variants: 85150944-G-A

http://identifiers.org/hco/22/GRCh38#45577994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#85150952-C-A

45577994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85150952-C-T

http://identifiers.org/hco/22/GRCh38#45578031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85150988-C-A

45578031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85150988-C-T

45578034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85150991-T-A

45578161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85151094-G-T

45578213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85151149-G-T

45578474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151410-T-A

http://identifiers.org/hco/22/GRCh38#45578538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85151437-C-A

45578620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151486-T-C

45578628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151494-G-C

45578704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151562-G-A

45578759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151593-G-A

45578964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151758-G-A

45579146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151925-C-T

45579211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85151983-C-T

45579546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85152303-G-T

45579755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85152493-G-A

45579816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85152557-C-T

45579864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85152601-C-G

45580057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85152795-G-A

45580478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153180-G-A

45580488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153186-G-A

45580670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153319-C-G

45580670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153319-C-T

45580743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153381-C-T

45580765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153413-G-A

45580783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153431-G-C

45580980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153639-C-T

45580981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153640-G-A

45581132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153770-G-A

45581139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85153777-G-C

45582914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85154998-C-T

45583073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155134-G-A

45583073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155134-G-T

45583111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155163-A-G

45583147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155182-A-T

http://identifiers.org/hco/22/GRCh38#45583235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85155252-C-A

45583235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155252-C-T

45583275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155290-A-G

http://identifiers.org/hco/22/GRCh38#45583702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85155672-A-C

45583766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155733-G-A

45583941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85155880-C-T

45584109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156011-C-G

45584109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156011-C-T

45584192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156093-A-G

45584485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156375-G-A

45584555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156448-C-T

45584617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156501-A-T

http://identifiers.org/hco/22/GRCh38#45584694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85156571-A-C

45584902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156756-T-A

45584902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156756-T-C

45584964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156817-G-C

45585148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85156979-T-C

45585234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85157057-G-A

45585549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85157344-G-A

45585737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85157526-G-A

45585790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85157587-C-T

45586525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85158140-A-G

45586741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85158352-G-C

45586769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85158380-C-T

45587038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85158613-A-G

45587787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85159060-T-A

http://identifiers.org/hco/22/GRCh38#45587815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85159085-C-A

45590814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161112-G-A

45590861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161155-G-A

45590968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161217-G-A

45591195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161414-C-T

45591196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161415-G-T

45591267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161499-T-G

45591594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161805-C-T

45591730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161938-G-C

45591738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85161946-C-T

45593005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85163428-C-T

45593039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85163454-C-T

45593197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85163590-A-G

45593208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85163601-A-G

http://identifiers.org/hco/22/GRCh38#45593282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85163665-C-A

45593406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85163784-A-G

45593606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85164389-T-G

45593673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85164446-G-A

45593673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85164446-G-C

45593840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85164613-T-C

45594465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85165678-C-T

45594881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85165978-G-C

45595303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85166366-G-A

45595519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85166547-C-T

45595523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85166553-T-C

45595547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85166578-G-A

45595608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85166646-G-A

45597393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85168255-C-G

45597566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85168423-G-A

45597728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron_variant, undefined
orthologous variants: 85168543-A-G

45597753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85168569-G-A

45597753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85168569-G-C

45597794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85168606-C-G

45600219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85169154-T-C

45600230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85169164-A-G

45600264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: intron variant
orthologous variants: 85169195-C-T

http://identifiers.org/hco/22/GRCh38#45600338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85169272-C-A

45600360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: synonymous variant
orthologous variants: 85169294-C-T

45600389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: synonymous variant
orthologous variants: 85169323-G-T

45600404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: synonymous variant
orthologous variants: 85169338-T-C

45600450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169384-C-T

http://identifiers.org/hco/22/GRCh38#45600458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85169391-C-A

45600458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169391-C-T

45600474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169412-G-T

45600486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169424-C-T

45600532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169470-C-T

45600575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169511-G-A

45600575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169511-G-C

45600575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169511-G-T

45600591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169527-G-T

45600651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169577-G-C

http://identifiers.org/hco/22/GRCh38#45600665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85169590-C-A

45600665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169590-C-T

45600695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169628-G-T

45600704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169637-T-A

45600717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169651-G-T

45600718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169652-G-A

45600718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169652-G-T

45600770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169700-A-G

http://identifiers.org/hco/22/GRCh38#45600792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85169716-C-A

45600792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169716-C-T

http://identifiers.org/hco/22/GRCh38#45600855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85169782-C-A

45600855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169782-C-T

45600887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169814-G-A

45600897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169824-A-G

http://identifiers.org/hco/22/GRCh38#45600943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85169874-C-A

45600943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3600
most severe consequence: 3 prime UTR variant
orthologous variants: 85169874-C-T