77696033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098926-G-T

77696333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098672-T-C

http://identifiers.org/hco/1/GRCh38#77696578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152098417-C-A

77696578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098417-C-G

77696689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098307-C-T

77696722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098274-G-T

77696783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098219-T-C

77697114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098187-A-G

77697260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098051-G-A

77697260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3 prime UTR variant
orthologous variants: 152098051-G-T

77697597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152097730-T-A

77697609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097718-G-T

77697622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097706-T-C

77697661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097666-G-A

77697661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097666-G-T

http://identifiers.org/hco/1/GRCh38#77697695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152097636-C-A

77697704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097627-G-A

77697704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097627-G-T

77697723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097610-C-G

77697723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097610-C-T

77697753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152097566-G-T

77697968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152097242-A-T

77697998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152097212-T-C

77698835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152096870-C-T

77698855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152096850-A-G

77698900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152096792-A-G

77700662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152096208-G-A

77700733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152096132-C-T

77700957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152095844-C-T

http://identifiers.org/hco/1/GRCh38#77701271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152095551-A-C

77701335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152095508-T-C

77701352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152095495-T-C

77701480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152095367-G-A

77701480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152095367-G-T

http://identifiers.org/hco/1/GRCh38#77701501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152095348-A-C

77701501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152095348-A-G

77702286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152095164-G-A

77711811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152089795-G-A

77711948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152089503-T-C

77712174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152089256-G-C

77712176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152089254-C-T

77712880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088977-A-G

77713055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088828-G-A

77713055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088828-G-T

http://identifiers.org/hco/1/GRCh38#77713057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152088826-C-A

77713057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088826-C-T

http://identifiers.org/hco/1/GRCh38#77713066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152088817-C-A

77713066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088817-C-T

77713116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088755-G-A

77713147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088714-A-T

77713453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152088498-G-T

77713477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152088485-T-C

77713534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088432-T-C

77713577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088398-T-G

77713578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088397-G-A

77713578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088397-G-T

77713596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088378-T-C

http://identifiers.org/hco/1/GRCh38#77713603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152088371-C-A

77713603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152088371-C-T

http://identifiers.org/hco/1/GRCh38#77713645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152088336-C-A

77714089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152087923-A-G

77714222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152087831-G-A

77714222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152087831-G-C

77714484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152087638-A-G

77714516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152087614-T-C

77714516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152087614-T-G

http://identifiers.org/hco/1/GRCh38#77714577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152087556-A-C

77714813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152087320-A-G

77715014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152087117-T-C

http://identifiers.org/hco/1/GRCh38#77715016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152087115-C-A

77715075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152087057-C-T

77715501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086489-G-A

77715518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086472-T-C

77715591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086406-A-G

77715592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086405-T-C

77715667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086343-T-A

77715706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086309-G-A

77715878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086143-A-G

77715889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086132-A-G

77715994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152086061-T-C

77716091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 152085974-C-T

77717590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152085384-G-T

77718010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152085108-A-G

77718225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152084799-A-G

77718381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152084634-G-A

77718388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152084626-T-C

77718388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152084626-T-G

77718652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152084468-A-G

77718720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152084399-A-G

77720238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152083126-A-G

77720238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152083126-A-T

77720242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152083122-T-C

77720363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152083020-C-T

77720503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152082844-T-C

77720503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152082844-T-G

77720688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152082462-G-A

77720801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152082226-C-T

77720882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152082155-G-A

77720991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152082061-A-G

http://identifiers.org/hco/1/GRCh38#77721090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152081990-C-A

77721096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152081984-T-A

77721156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152081924-T-A

77721156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152081924-T-C

77721162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152081920-T-C

77721162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152081920-T-G

77721208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 152081874-G-A

77721252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152081832-T-C

77721252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152081832-T-G

77721294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152081817-G-T

77721308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152081803-G-A

http://identifiers.org/hco/1/GRCh38#77721404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152081722-C-A

77721787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152080654-A-G

http://identifiers.org/hco/1/GRCh38#77721809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152080637-C-A

77721809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152080637-C-T

77721857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152080594-G-A

77722003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152080445-A-G

77722004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152080444-C-G

77722111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152080340-T-A

77722111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152080340-T-C

77722111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152080340-T-G

77722120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 152080331-G-T

77722192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152080259-G-C

77722227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152080229-T-C

http://identifiers.org/hco/1/GRCh38#77722309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152080145-A-C

77722393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152080103-T-C

77722393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152080103-T-G

http://identifiers.org/hco/1/GRCh38#77722485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152080007-A-C

77722485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152080007-A-G

77722489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152080003-A-G

77722896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079503-T-A

77722898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079501-T-C

77722943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079477-T-C

77723194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079268-G-A

77723194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079268-G-T

77723208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079247-A-G

77723218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079237-T-C

77723219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079236-G-T

77723227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079228-A-T

77723297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079164-A-G

77723297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079164-A-T

77723315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152079148-A-G

77725267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152076523-C-T

77725489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152076171-T-C

77725599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152076074-A-T

http://identifiers.org/hco/1/GRCh38#77725740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152075934-C-A

77725740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: synonymous variant
orthologous variants: 152075934-C-G

77725740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: synonymous variant
orthologous variants: 152075934-C-T

http://identifiers.org/hco/1/GRCh38#77725803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152075874-A-C

http://identifiers.org/hco/1/GRCh38#77727326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152075320-A-C

77727326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152075320-A-T

http://identifiers.org/hco/1/GRCh38#77727440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152075226-C-A

77727456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152075210-T-A

77727512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152075161-C-T

77727955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074789-T-C

77728038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074714-T-C

77728109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074650-T-C

77728215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074513-C-T

http://identifiers.org/hco/1/GRCh38#77728220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152074508-A-C

77728240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074372-C-T

77728243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074335-T-A

77728243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152074335-T-C

77728561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense variant
orthologous variants: 152074022-C-T

77729526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152072650-C-G

77730510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152072057-T-C

77730636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: missense variant
orthologous variants: 152071944-T-C

77730882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152071698-G-C

http://identifiers.org/hco/1/GRCh38#77730910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152071676-C-A

77730910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152071676-C-T

77731044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152071244-T-C

77731068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152071223-T-A

77731068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152071223-T-C

77734329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069700-A-G

77734331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069698-T-A

77734331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069698-T-C

77734413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 152069616-A-G

77734444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069589-A-T

77734483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069426-T-C

77734484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069425-T-A

77734578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152069327-A-G

77735828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067855-T-C

77735908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067771-A-G

http://identifiers.org/hco/1/GRCh38#77735926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152067753-A-C

77735926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067753-A-G

77735930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067749-T-C

http://identifiers.org/hco/1/GRCh38#77735932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152067747-C-A

77735932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067747-C-T

77736005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067686-T-C

77736018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067673-A-G

http://identifiers.org/hco/1/GRCh38#77736022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152067669-C-A

77736022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067669-C-T

77736050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067643-A-G

77736051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067642-T-C

http://identifiers.org/hco/1/GRCh38#77736118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152067575-A-C

77736172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067523-A-G

http://identifiers.org/hco/1/GRCh38#77736190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152067505-C-A

77736190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067505-C-G

77736199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067496-A-G

http://identifiers.org/hco/1/GRCh38#77736200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152067495-A-C

77736200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067495-A-T

77736245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067448-T-C

77736276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152067413-G-T

77739194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152066128-A-G

77739194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron variant
orthologous variants: 152066128-A-T

http://identifiers.org/hco/1/GRCh38#77739510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152065832-C-A

77739510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152065832-C-T

77739568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152065761-G-A

77739568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152065761-G-T

http://identifiers.org/hco/1/GRCh38#77739754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152065486-A-C

77740016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152065233-A-G

77740247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152065020-G-A

77740754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064633-G-A

http://identifiers.org/hco/1/GRCh38#77740788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152064469-C-A

77740804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064456-T-A

77740831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064430-G-C

77740831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064430-G-T

77740847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064381-A-G

77740847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064381-A-T

77740858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064368-A-T

77740908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152064302-G-A

77740908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 152064302-G-C

77740908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 152064302-G-T

77740989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064230-G-A

77740989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152064230-G-T

http://identifiers.org/hco/1/GRCh38#77741047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152064173-C-A

77741229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063992-T-A

77741229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063992-T-G

http://identifiers.org/hco/1/GRCh38#77741263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152063956-C-A

77741266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063953-G-T

77741301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063922-T-A

77741307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063921-G-A

77741307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063921-G-T

77741356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063877-A-G

http://identifiers.org/hco/1/GRCh38#77741430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152063780-C-A

http://identifiers.org/hco/1/GRCh38#77741470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152063743-C-A

77741470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063743-C-G

77741470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063743-C-T

http://identifiers.org/hco/1/GRCh38#77741476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152063734-C-A

77741476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063734-C-T

77741486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063724-T-C

77741518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063701-T-C

77741537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063687-G-C

77741564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063661-C-T

77741582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063641-A-G

77741743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 152063480-T-C

77741839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152063431-T-G

77754990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152057414-C-T

77757856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152053820-C-T

77758006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152053748-T-C

http://identifiers.org/hco/1/GRCh38#77758075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152053684-C-A

77759355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152052402-T-C

http://identifiers.org/hco/1/GRCh38#77759550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152052301-C-A

77759550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152052301-C-T

77759615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152052295-G-A

77759615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152052295-G-T

http://identifiers.org/hco/1/GRCh38#77759618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152052292-C-A

77759618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152052292-C-T

http://identifiers.org/hco/1/GRCh38#77759842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20059
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152052141-C-A