76142622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116227379-C-T

76142648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116227407-A-G

76142648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116227407-A-T

http://identifiers.org/hco/17/GRCh38#76142803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116227531-C-A

76142803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116227531-C-T

76142859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116227582-G-A

76142859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116227582-G-T

76142898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116227618-G-A

76143258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116227850-G-A

76143258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116227850-G-T

http://identifiers.org/hco/17/GRCh38#76143383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116227996-C-A

76143383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116227996-C-T

http://identifiers.org/hco/17/GRCh38#76143412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116228022-C-A

76143421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116228031-A-T

76143457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116228060-A-G

76143470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116228064-A-G

76143480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116228074-G-T

76143525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116228131-A-G

76143545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116228151-G-A

76143545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116228151-G-T

76143550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116228156-G-T

http://identifiers.org/hco/17/GRCh38#76143554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116228160-A-C

76144719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229066-T-A

76144873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229195-T-G

http://identifiers.org/hco/17/GRCh38#76144893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116229215-C-A

76145098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229364-T-G

76145158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229450-A-G

76145213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229508-G-T

76145302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229602-C-T

76145410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229713-T-A

76145410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229713-T-C

76145410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116229713-T-G

76145739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116229999-G-C

76145881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230125-G-A

76145921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230153-C-T

76145927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230159-C-T

76146150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230297-T-C

http://identifiers.org/hco/17/GRCh38#76146208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116230350-C-A

76146289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116230432-T-C

76146323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116230472-A-G

76146324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116230473-G-A

76146324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116230473-G-T

76146406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230544-G-A

76146406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230544-G-T

76146581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230692-C-G

76146589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230700-C-T

http://identifiers.org/hco/17/GRCh38#76146895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116230873-C-A

76146902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230880-T-C

76146920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230901-T-C

76147019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116230984-G-C

76147115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231041-T-G

http://identifiers.org/hco/17/GRCh38#76147232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116231127-C-A

76147232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231127-C-T

76147279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116231174-A-G

76147364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231259-G-A

76147364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231259-G-T

76147388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231285-A-G

76147394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231291-A-G

76147400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231297-A-G

76147427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231323-T-C

76147484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231362-A-G

76147497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231377-A-G

76147497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231377-A-T

76147553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231418-T-A

76147553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116231418-T-C

76147601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116231451-T-C

76147632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231472-A-G

76147634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231474-C-T

http://identifiers.org/hco/17/GRCh38#76147687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116231526-C-A

76147687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231526-C-T

http://identifiers.org/hco/17/GRCh38#76147821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116231632-A-C

76147821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116231632-A-G

76148914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116232395-G-T

76148952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116232427-G-T

76149400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116232781-C-T

76149482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116232861-G-T

76150347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116233199-G-A

http://identifiers.org/hco/17/GRCh38#76150372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116233234-C-A

76150372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116233234-C-T

76150702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116233518-C-T

76150843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116233643-G-A

76151036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116233850-C-T

76151112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116233923-G-A

76152303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116234970-G-C

76152303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116234970-G-T

http://identifiers.org/hco/17/GRCh38#76152315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116234981-C-A

76152315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116234981-C-T

76152519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116235184-T-C

76152588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235273-A-G

http://identifiers.org/hco/17/GRCh38#76152625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116235354-C-A

76152652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235380-C-T

76152655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235385-G-A

76152655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235385-G-T

76153001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235722-T-G

76153052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235773-T-C

http://identifiers.org/hco/17/GRCh38#76153054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116235775-C-A

76153093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235813-T-A

http://identifiers.org/hco/17/GRCh38#76153109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116235829-C-A

76153109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116235829-C-T

76153158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235873-G-A

76153158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235873-G-T

76153170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235886-G-A

http://identifiers.org/hco/17/GRCh38#76153198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116235915-C-A

76153236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235949-A-G

76153236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235949-A-T

http://identifiers.org/hco/17/GRCh38#76153262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116235967-C-A

76153285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235979-G-C

76153285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116235979-G-T

http://identifiers.org/hco/17/GRCh38#76153519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236152-C-A

76153519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116236152-C-T

http://identifiers.org/hco/17/GRCh38#76153586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236205-C-A

76153586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116236205-C-T

76153778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116236355-C-T

http://identifiers.org/hco/17/GRCh38#76153779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236356-C-A

76153809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236386-G-A

76153810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236387-T-C

76153810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236387-T-G

http://identifiers.org/hco/17/GRCh38#76153839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236401-C-A

76153839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236401-C-T

http://identifiers.org/hco/17/GRCh38#76153840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236402-C-A

76153848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236410-A-G

http://identifiers.org/hco/17/GRCh38#76153867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236428-C-A

76153867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236428-C-G

76153867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236428-C-T

76154004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236508-C-G

76154004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116236508-C-T

http://identifiers.org/hco/17/GRCh38#76154058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236539-C-A

76154058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116236539-C-G

76154058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116236539-C-T

http://identifiers.org/hco/17/GRCh38#76154177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236634-C-A

76154181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116236638-G-A

76154181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116236638-G-T

http://identifiers.org/hco/17/GRCh38#76154229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236687-A-C

76154279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116236732-C-G

76154279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116236732-C-T

76154316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236769-T-C

76154358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236811-A-G

http://identifiers.org/hco/17/GRCh38#76154412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116236858-C-A

76154412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236858-C-T

76154414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236860-G-A

76154414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236860-G-C

76154414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236860-G-T

76154441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236886-T-A

76154441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236886-T-C

76154441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116236886-T-G

http://identifiers.org/hco/17/GRCh38#76155102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116237724-C-A

76155102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237724-C-G

76155144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237761-G-A

76155144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237761-G-C

76155144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237761-G-T

http://identifiers.org/hco/17/GRCh38#76155178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116237782-A-C

76155178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237782-A-G

76155178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237782-A-T

76155211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237820-G-C

76155211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237820-G-T

76155213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237822-T-C

76155213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237822-T-G

76155285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116237892-A-G

76155326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237933-G-A

76155326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237933-G-C

http://identifiers.org/hco/17/GRCh38#76155367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116237990-A-C

76155367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116237990-A-G

76155413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238043-G-A

76155413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238043-G-T

76155431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238058-G-A

76155431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238058-G-T

76155457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238087-A-T

http://identifiers.org/hco/17/GRCh38#76155512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116238123-A-C

76155548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238154-G-A

76155577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116238180-G-A

76155577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116238180-G-C

76155577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116238180-G-T

76155597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116238200-G-A

76155597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116238200-G-C

76155613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116238216-C-T

76155836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238422-G-A

76155836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238422-G-T

http://identifiers.org/hco/17/GRCh38#76155856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116238442-C-A

76155888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238473-T-C

76155975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238536-G-C

76156166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238646-G-T

76156183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116238661-T-C

http://identifiers.org/hco/17/GRCh38#76156423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116238880-A-C

76156450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116238906-A-G

76156451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116238907-T-C

76156451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116238907-T-G

76156502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116238962-A-G

76156600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116239057-C-T

76158235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116240014-T-C

76158251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116240030-G-A

76158256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116240035-A-G

76158261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116240040-T-C

76158353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116240121-G-A

76158353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116240121-G-T

76158444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116240211-G-A

76158444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116240211-G-C

76158510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116240277-G-A

76158510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116240277-G-T

http://identifiers.org/hco/17/GRCh38#76159285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116240722-C-A

76159316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116240753-T-C

76159499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: synonymous variant
orthologous variants: 116240950-G-T

76159606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241056-T-C

76159681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241132-G-A

76159681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241132-G-C

76159684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241135-G-A

76159684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241135-G-T

76159788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241223-T-A

76159934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116241363-T-C

76161099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116244209-A-G

76161187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116244306-C-T

http://identifiers.org/hco/17/GRCh38#76161266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116244382-C-A

76161290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116244405-T-C

76161332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116244447-A-G

76161490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116245146-T-G

76161777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116245432-G-C

76162092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116245707-A-G

76162109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116245718-A-G

http://identifiers.org/hco/17/GRCh38#76162182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116245773-A-C

76162182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116245773-A-G

http://identifiers.org/hco/17/GRCh38#76162197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116245788-A-C

76162515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246234-T-C

76162539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246258-G-T

76162549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246268-T-C

76162645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246364-T-C

76162674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246391-A-G

76162725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246435-G-A

76162725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246435-G-C

76162725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116246435-G-T

76162763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116246464-T-A

http://identifiers.org/hco/17/GRCh38#76162899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116246588-C-A

76162899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116246588-C-T

76164133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116248927-G-A

76164133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116248927-G-C

76164133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116248927-G-T

http://identifiers.org/hco/17/GRCh38#76164134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116248928-C-A

76164134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116248928-C-T

76164202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116248993-G-T

76164213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116249004-G-A

76164531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116249314-A-G

76164538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116249321-T-A

76164538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116249321-T-C

http://identifiers.org/hco/17/GRCh38#76164629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116249403-A-C

76164629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116249403-A-G

76164629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116249403-A-T

76165391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116249686-T-A

76165392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116249687-A-G

76165411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116249706-T-C

76165412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116249707-G-A

http://identifiers.org/hco/17/GRCh38#76165581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116249838-A-C

76166498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: stop_gained, undefined
orthologous variants: 116250106-G-T

76166533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116250141-G-A

76166545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250152-G-A

http://identifiers.org/hco/17/GRCh38#76166565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250172-C-A

76166565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250172-C-T

76166568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250222-A-G

76166570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250224-C-G

76166576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250230-T-C

http://identifiers.org/hco/17/GRCh38#76166578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250232-C-A

76166597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250254-G-T

http://identifiers.org/hco/17/GRCh38#76166620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250277-C-A

http://identifiers.org/hco/17/GRCh38#76166634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250291-C-A

http://identifiers.org/hco/17/GRCh38#76166646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250302-C-A

76166831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250487-A-G

http://identifiers.org/hco/17/GRCh38#76166885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250541-C-A

76166886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250542-A-T

76166906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250562-G-A

76166906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250562-G-C

76166906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250562-G-T

76167090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: synonymous variant
orthologous variants: 116250720-A-T

76167182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250809-G-A

76167182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250809-G-T

http://identifiers.org/hco/17/GRCh38#76167187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116250814-C-A

76167211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250839-A-G

76167267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250895-T-C

76167268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250896-G-A

76167305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250936-C-T

76167348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250954-G-A

76167357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250963-C-T

76167461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116250992-G-A

76167469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116251000-C-T

76167470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116251001-T-C

76167489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116251021-T-C

76167503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116251029-T-A

76167710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: synonymous variant
orthologous variants: 116251139-A-G

76173393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116252804-A-T

76173566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116252992-C-T

http://identifiers.org/hco/17/GRCh38#76173578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116253002-C-A

76173578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253002-C-T

76173639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253059-C-G

76173639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253059-C-T

76173686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253095-G-A

76173686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253095-G-C

76173686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253095-G-T

76173832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253238-A-G

http://identifiers.org/hco/17/GRCh38#76173933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116253333-C-A

76173933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253333-C-G

76173933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253333-C-T

76174076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253492-T-A

76174157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253585-C-T

76174162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253590-A-G

76174211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253617-G-A

76174368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116253755-G-A

76174415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, undefined
orthologous variants: 116253793-C-T

76174759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116254287-G-C

76180741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258187-G-C

76180758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258201-A-G

76181170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258551-C-T

76181217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258615-G-A

76181217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258615-G-C

76181254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258650-C-T

76181297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116258690-T-C

76182434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, undefined
orthologous variants: 116259219-G-T

76182613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, undefined
orthologous variants: 116259491-T-C

76182618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, undefined
orthologous variants: 116259496-A-G

http://identifiers.org/hco/17/GRCh38#76183927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116261788-C-A

76183947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116261807-T-C

76183995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116261875-G-C

76184023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116261903-C-T

76184121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262017-G-A

76184208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262081-G-A

76184717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262515-C-T

76184720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262518-T-C

76184811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262602-A-G

76184875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262664-C-T

76184995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262779-T-C

76185049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116262835-T-C

76186009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116263591-T-C

76186019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116263601-T-C

76186057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116263624-G-A

76187934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264428-T-C

76187935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264429-G-A

76187943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264437-A-G

76187989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264479-C-T

76187999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264489-T-A

76188049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264534-T-C

76188166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264647-G-C

76188343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264815-C-T

76188348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264820-T-C

76188474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264945-C-T

76188477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264948-T-C

76188494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116264965-G-A

76188711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116265418-G-A

76188711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116265418-G-C

76188739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116265446-T-C

76188802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116265502-G-T

76188845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116265545-T-C

76192073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116268044-G-A

76192453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116268362-G-A

76192573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116268436-A-G

76192638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116268492-A-G

76193043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116268740-T-C

76193043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116268740-T-G

76197148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116271505-T-G

76197213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116271569-G-A

76197213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116271569-G-T

76197218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116271573-T-C

76197754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116271776-T-A

76198159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116272471-T-A

76198532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116272647-A-G

76198547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116272662-C-G

76198776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116273043-C-T

76199100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116273380-G-A

76206398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116277404-G-T

76206475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116277446-C-T

76206488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116277459-T-G

76206858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116277826-T-C

http://identifiers.org/hco/17/GRCh38#76207534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116278203-C-A

76207601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116278261-T-G

76207614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116278277-A-G

76209317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116279856-A-G

76212430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: synonymous variant
orthologous variants: 116287081-A-G

76212949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116287265-C-T

76213281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116288110-A-G

76215011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116288803-A-T

76215109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116288895-G-A

76215134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116288918-T-C

76215618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116289016-T-C

76237941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301197-G-A

76237951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301207-G-A

76237992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, undefined
orthologous variants: 116301247-G-A

76238017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301257-G-T

76238037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron_variant, undefined
orthologous variants: 116301277-T-C

76238056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301300-C-G

76238065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301309-G-A

http://identifiers.org/hco/17/GRCh38#76238083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116301334-C-A

76238083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301334-C-T

76238661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116301972-A-G

http://identifiers.org/hco/17/GRCh38#76239120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116302708-C-A

76239168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116302757-A-T

http://identifiers.org/hco/17/GRCh38#76239217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116302793-C-A

76239238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116302824-T-C

76239254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116302846-T-C

http://identifiers.org/hco/17/GRCh38#76239255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116302847-A-C

76239255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116302847-A-G

76239958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303350-G-A

76239958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303350-G-T

76239970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303366-A-T

76240026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303425-A-T

76240036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303435-A-G

http://identifiers.org/hco/17/GRCh38#76240094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116303476-C-A

76240094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303476-C-T

http://identifiers.org/hco/17/GRCh38#76240133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116303502-C-A

76240133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: intron variant
orthologous variants: 116303502-C-T

76240166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: synonymous variant
orthologous variants: 116303536-G-A

76240166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: stop gained
orthologous variants: 116303536-G-T

76240332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 5 prime UTR variant
orthologous variants: 116303690-G-A

76240332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 5 prime UTR variant
orthologous variants: 116303690-G-T

76240339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 5 prime UTR variant
orthologous variants: 116303697-G-A

76240339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29402
most severe consequence: 5 prime UTR variant
orthologous variants: 116303697-G-T