197671654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32641863-G-A

197671939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642035-T-A

197671967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642066-T-C

197672135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642230-G-A

197672139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642234-A-G

197672168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642264-C-T

http://identifiers.org/hco/3/GRCh38#197672427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32642419-C-A

197672427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642419-C-G

197672427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642419-C-T

http://identifiers.org/hco/3/GRCh38#197672456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32642450-A-C

197672456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642450-A-T

197672471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642463-C-T

197672495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642485-G-A

197672495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642485-G-T

197672520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642510-G-A

197672531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642519-T-C

197673282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642835-T-C

197673282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32642835-T-G

http://identifiers.org/hco/3/GRCh38#197673311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32642862-C-A

197673623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643151-G-T

197673740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643196-G-A

197673740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643196-G-T

197673796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643256-T-C

197673880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643320-T-C

197673986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643423-A-G

197674088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643524-T-C

197674089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643525-G-A

197674089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643525-G-T

197674107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643543-T-G

197674123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643558-G-T

197674202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643630-A-G

197674212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643636-T-C

197674213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643637-G-A

197674242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643665-G-T

http://identifiers.org/hco/3/GRCh38#197674296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32643703-A-C

http://identifiers.org/hco/3/GRCh38#197674365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32643765-C-A

http://identifiers.org/hco/3/GRCh38#197674493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32643884-C-A

197674493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32643884-C-T

http://identifiers.org/hco/3/GRCh38#197674543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32643931-C-A

197674625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32644022-G-A

197674625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32644022-G-T

197674676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32644067-G-A

197674676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32644067-G-T

197674690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32644092-A-G

197675186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32644506-C-G

197675186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32644506-C-T

197675237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644557-T-A

http://identifiers.org/hco/3/GRCh38#197675271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32644591-C-A

197675271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644591-C-T

197675275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644595-C-T

197675277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644597-C-G

197675283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644603-G-A

197675283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644603-G-T

197675284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644604-C-T

197675363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644710-G-T

197675595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644909-G-A

197675595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644909-G-T

197675631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32644962-G-T

197675795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645118-G-A

http://identifiers.org/hco/3/GRCh38#197675868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32645186-A-C

197675964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645271-T-A

197675964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645271-T-C

http://identifiers.org/hco/3/GRCh38#197676094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32645355-C-A

197676094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645355-C-T

http://identifiers.org/hco/3/GRCh38#197676107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32645363-C-A

197676107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645363-C-T

197676110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645366-A-G

197676173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645425-T-C

197676211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32645471-G-C

197676358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645559-G-C

197676358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645559-G-T

http://identifiers.org/hco/3/GRCh38#197676380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32645566-C-A

197676380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645566-C-T

197676390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645576-T-A

197676390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645576-T-C

197676471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645608-G-A

197676471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645608-G-T

197676481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645618-T-C

197676481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645618-T-G

http://identifiers.org/hco/3/GRCh38#197676669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32645697-C-A

197676669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645697-C-T

http://identifiers.org/hco/3/GRCh38#197676676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32645704-C-A

197676676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645704-C-T

197676705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645733-G-C

197676705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645733-G-T

197676781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645806-A-G

197676781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645806-A-T

197676802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645820-G-A

197676802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32645820-G-C

197676868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, missense_variant
orthologous variants: 32645917-C-T

197676897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32645946-C-T

197676963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32646012-A-G

197676981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32646030-G-A

197676990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32646039-G-A

197676990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32646039-G-C

197677042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32646091-C-T

197677045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32646097-G-A

197677045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32646097-G-T

197677077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32646137-G-C

http://identifiers.org/hco/3/GRCh38#197677359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32646360-C-A

197677366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32646370-G-T

197677416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32646440-C-T

197677454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32646477-A-G

197677555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32646580-G-T

197681213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32647139-A-G

197681213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32647139-A-T

197681410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647331-A-G

197681413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647334-T-G

http://identifiers.org/hco/3/GRCh38#197681443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32647349-C-A

http://identifiers.org/hco/3/GRCh38#197681462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32647368-A-C

197681699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647556-T-C

197681709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647566-T-G

197681715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647569-T-A

197681715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647569-T-C

197681804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647637-A-T

http://identifiers.org/hco/3/GRCh38#197681842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32647665-A-C

http://identifiers.org/hco/3/GRCh38#197681973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32647795-C-A

197681973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647795-C-T

197681990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647807-A-G

197682029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32647847-A-T

http://identifiers.org/hco/3/GRCh38#197682337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32648104-C-A

197682337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648104-C-G

197682337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648104-C-T

197682356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648123-G-A

197682356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648123-G-T

197682411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648182-C-T

http://identifiers.org/hco/3/GRCh38#197682511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32648270-C-A

197682511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32648270-C-T

197682538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32648297-A-G

197682610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32648369-C-T

197682639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648393-G-C

197682653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648321-A-G

197682698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648366-G-A

197682748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648424-A-G

197682844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648526-A-G

197682906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648584-C-T

197683080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648769-C-T

197683162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648893-T-C

197683186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648918-G-A

197683186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648918-G-T

197683202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648935-G-A

197683222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32648954-C-T

197683299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32649031-G-A

197683484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649211-G-A

197683525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649224-A-G

197683558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649259-C-T

197683566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649267-T-A

197683588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649291-G-C

197683588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649291-G-T

197684071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649559-G-A

197684071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649559-G-T

http://identifiers.org/hco/3/GRCh38#197684091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32649579-C-A

197684091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649579-C-G

http://identifiers.org/hco/3/GRCh38#197684109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32649597-A-C

197684109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649597-A-G

197684256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649727-C-G

197684256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649727-C-T

197684259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649730-G-A

197684259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649730-G-T

197684277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649749-G-A

197684277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649749-G-C

197684277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649749-G-T

197684423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649893-T-C

http://identifiers.org/hco/3/GRCh38#197684473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32649940-A-C

197684480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649947-G-A

197684819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650231-T-C

197685014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650384-G-C

197685500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650819-T-A

197685575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650891-A-G

197685575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650891-A-T

197685608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650924-A-G

197685650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651033-T-C

197685690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651077-G-A

197686017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651405-G-A

http://identifiers.org/hco/3/GRCh38#197686533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32652051-C-A

197686533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652051-C-T

197686536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652054-C-T

197686675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652171-G-A

197686911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652338-T-G

197686974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652393-A-G

197687189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652515-C-G

197690775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653765-G-A

197690951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653891-T-C

http://identifiers.org/hco/3/GRCh38#197690960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32653900-C-A

197690960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653900-C-T

197690996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653936-A-G

197691031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653972-C-T

http://identifiers.org/hco/3/GRCh38#197691032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32653973-A-C

197691032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653973-A-T

197691048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653989-A-G

197691059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654000-T-G

197691101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32654041-A-G

http://identifiers.org/hco/3/GRCh38#197691140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#32654080-C-A

197691140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32654080-C-T

197691160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654100-T-C

197691217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654132-A-G

http://identifiers.org/hco/3/GRCh38#197691276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32654169-C-A

197691276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654169-C-T

197692662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654747-C-G

197692757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654831-C-T

197692852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654899-G-C

197692861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654908-A-T

197692906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654943-T-C

197693318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32655906-A-T

197693340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32655947-T-C

197693527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656117-C-T

197693564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656134-G-T

197693571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656137-G-A

197693571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656137-G-T

197693581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656147-G-T

http://identifiers.org/hco/3/GRCh38#197693582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32656148-A-C

197693582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656148-A-G

197693582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656148-A-T

197693687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656256-T-C

197693778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32656347-G-A

197693879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32656401-T-C

197694046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656458-T-G

197694203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656557-A-G

197694203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656557-A-T

197694303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656675-T-C

http://identifiers.org/hco/3/GRCh38#197694312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32656684-C-A

197694312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656684-C-T

http://identifiers.org/hco/3/GRCh38#197694319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32656691-C-A

197694319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656691-C-T

197694326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656698-C-G

197694326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656698-C-T

197694331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656703-G-A

197694331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32656703-G-T

197694562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32656967-T-C

197694574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32656979-G-A

197694574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense variant
orthologous variants: 32656979-G-C

197694580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32656985-A-G

197694675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32657089-G-C

197694710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32657120-G-C

197694710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32657120-G-T

197694737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32657147-G-T

197694811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32657207-A-G

197694836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32657240-C-T

197695494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658245-G-A

197695494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658245-G-C

197695494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658245-G-T

197695527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658269-G-C

197695542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658284-A-T

197695543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658285-G-T

197695594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658334-C-G

197695698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658433-T-C

197695700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658435-C-T

197695736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658467-G-A

197695736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658467-G-C

197695736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658467-G-T

197695753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658478-A-G

197695957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense variant
orthologous variants: 32658699-C-T

197696036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658807-C-T

197696111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658874-T-A

197696111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32658874-T-C

197696466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659125-G-A

197696520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659179-C-T

197696545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659204-T-C

197696837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659429-T-C

197696875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659457-C-G

http://identifiers.org/hco/3/GRCh38#197696881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32659463-C-A

197696909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659491-G-T

197696930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659509-A-G

197696930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659509-A-T

197697015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32659596-A-G

197697216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659743-G-A

197697225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32659752-A-G

197697416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660086-G-A

197697601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660274-C-T

197697607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660280-G-A

197697607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660280-G-T

197697641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660327-C-T

197697736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660465-A-G

197698011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32660984-G-A

197698101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32661067-C-T

http://identifiers.org/hco/3/GRCh38#197698273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32661222-C-A

197698350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32661290-C-G

197698456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32661393-A-G

197699290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32662007-A-G

197699728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32662542-C-T

http://identifiers.org/hco/3/GRCh38#197699749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32662563-A-C

http://identifiers.org/hco/3/GRCh38#197699965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32662774-C-A

197699965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32662774-C-T

http://identifiers.org/hco/3/GRCh38#197700068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32662848-C-A

197700068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32662848-C-T

197700416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32663177-A-G

http://identifiers.org/hco/3/GRCh38#197700427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32663188-C-A

197700483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32663237-A-G

http://identifiers.org/hco/3/GRCh38#197700530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32663285-A-C

197700530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32663285-A-G

197700585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, missense_variant
orthologous variants: 32663340-C-T

197700601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, missense_variant
orthologous variants: 32663356-G-A

197700630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense variant
orthologous variants: 32663385-G-A

197700908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32663663-A-T

http://identifiers.org/hco/3/GRCh38#197700998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32663753-A-C

197700998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32663753-A-G

197701047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense variant
orthologous variants: 32663802-G-A

197701124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32663879-T-C

197701157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32663912-A-G

197701175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32663926-A-G

197701200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32663952-G-A

197701200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32663952-G-T

http://identifiers.org/hco/3/GRCh38#197701248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32664004-A-C

197701277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32664027-T-C

197701298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32664041-G-A

197701298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32664041-G-T

197701339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32664083-C-T

197701528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron variant
orthologous variants: 32664279-T-C

197701701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32664910-C-T

197701727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32664942-G-A

197701727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32664942-G-C

197701727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: synonymous variant
orthologous variants: 32664942-G-T

197701788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32665000-G-A

197701788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32665000-G-T

197701802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32665014-G-A

http://identifiers.org/hco/3/GRCh38#197701845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32665057-C-A

197701845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32665057-C-T

197701891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32665113-T-C

197701964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32665183-T-C

197701964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32665183-T-G

197701973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32665194-G-A

197703463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667498-A-G

197703495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667535-T-G

197703536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667575-T-C

197703537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667576-G-T

197703543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667582-T-C

197703551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32667590-G-A

197703551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32667590-G-T

197703560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32667599-G-A

197703560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32667599-G-T

197703698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667731-G-T

197703731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667772-A-G

197703802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667833-G-A

197703802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667833-G-T

197703824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667848-G-A

197703873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667897-G-A

197703970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32667956-A-G

197704025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32668000-G-C

197704025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32668000-G-T

197704037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32668010-G-A

197704079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32668043-G-C

197704615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32668273-C-T

http://identifiers.org/hco/3/GRCh38#197704644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32668302-C-A

197705085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32670041-C-G

197705085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32670041-C-T

197705116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32670072-G-A

http://identifiers.org/hco/3/GRCh38#197712089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32673690-A-C

197712195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32673777-A-G

197712326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32673896-T-C

http://identifiers.org/hco/3/GRCh38#197712861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32674336-C-A

197713106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32674390-G-A

197713285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32674514-T-C

197713688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32674905-T-C

197716766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676133-G-A

197716848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676228-C-T

197716908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676280-A-T

http://identifiers.org/hco/3/GRCh38#197717148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32676544-C-A

197717148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676544-C-G

197717159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676555-G-A

http://identifiers.org/hco/3/GRCh38#197717201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32676610-A-C

197717201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676610-A-G

197717250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676646-T-C

197717253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676649-C-T

197717260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676656-G-A

197717309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676698-T-C

197717349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32676740-C-G

197717581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32677000-G-A

197717618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32677025-G-C

197717662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32677065-T-C

197717986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32677271-G-A

197717986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32677271-G-C

197718031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32677316-C-T

197718091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32677376-C-T

197718127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32677412-C-T

http://identifiers.org/hco/3/GRCh38#197718235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32677533-A-C

http://identifiers.org/hco/3/GRCh38#197718236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32677534-C-A

197718236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32677534-C-T

http://identifiers.org/hco/3/GRCh38#197718799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32677869-A-C

197719193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32679837-G-A

197719780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32680057-T-C

197724133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32680774-G-A

197724667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682091-G-A

http://identifiers.org/hco/3/GRCh38#197724844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32682264-A-C

197724844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682264-A-G

197724897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682319-A-T

197725097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682535-T-C

197725132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32682572-G-C

197725866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683145-T-A

197725866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683145-T-C

197725877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683156-C-G

197725897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683171-C-T

197725936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683214-A-G

197725948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683226-A-G

197725957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683235-T-C

197726131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32683406-C-G

197730018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684705-T-A

197730018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684705-T-C

197730128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684774-G-A

197730162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684808-C-T

197730304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32684935-C-G

197730475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685075-A-G

197732033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685316-G-A

197732033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685316-G-C

197732803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32685704-G-A

197733276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686086-T-C

197733277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686087-G-A

197733277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686087-G-C

197733715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686346-C-T

197733841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686729-G-T

197734484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686878-T-C

http://identifiers.org/hco/3/GRCh38#197734568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32686962-C-A

197734573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32686967-G-A

197734812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687240-A-T

197735897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687719-G-A

http://identifiers.org/hco/3/GRCh38#197735976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32687804-C-A

197736062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32687878-C-T

197736270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688073-C-T

197736434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688243-G-C

http://identifiers.org/hco/3/GRCh38#197736480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32688299-A-C

http://identifiers.org/hco/3/GRCh38#197736534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32688352-C-A

197736534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688352-C-T

http://identifiers.org/hco/3/GRCh38#197736537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32688355-C-A

197736537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688355-C-T

http://identifiers.org/hco/3/GRCh38#197736571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32688388-C-A

197736571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32688388-C-T

197736707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688518-C-T

197736780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688589-G-A

197736868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688676-G-A

197736868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688676-G-T

197737117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688821-G-A

197737117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688821-G-T

197737178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688902-G-A

197737178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688902-G-T

197737246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32688959-G-A

http://identifiers.org/hco/3/GRCh38#197737347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32689059-C-A

197737347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32689059-C-T

197737611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32689763-G-A

197738113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690374-T-G

197738157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690400-C-G

http://identifiers.org/hco/3/GRCh38#197738204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32690447-C-A

197738275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690512-T-C

http://identifiers.org/hco/3/GRCh38#197738297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32690534-A-C

197738355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32690592-G-A

197746654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693342-C-T

http://identifiers.org/hco/3/GRCh38#197746814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32693501-A-C

http://identifiers.org/hco/3/GRCh38#197746815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32693502-C-A

197746815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693502-C-T

197746946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693632-C-G

197746946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32693632-C-T

197748243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32696456-G-A

197748249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32696462-A-G

http://identifiers.org/hco/3/GRCh38#197748301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32696508-C-A

197748600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32696960-T-C

197748647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697000-A-G

197748721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697081-G-C

197748829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697192-T-C

197748950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697322-A-T

197749228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697592-G-A

197749228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32697592-G-T

197749285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697648-T-G

http://identifiers.org/hco/3/GRCh38#197749315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32697678-C-A

197749315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697678-C-T

197749335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32697698-G-T

197749348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697711-T-C

197749477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697801-G-A

197749477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697801-G-C

197749480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697804-G-A

197749480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697804-G-C

197749480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697804-G-T

197749481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697805-A-G

197749481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697805-A-T

197749490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697814-G-A

http://identifiers.org/hco/3/GRCh38#197749522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32697848-C-A

197749522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697848-C-G

http://identifiers.org/hco/3/GRCh38#197749530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#32697856-C-A

197749530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697856-C-G

197749530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32697856-C-T

197749581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32697883-G-A

197749581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 32697883-G-T

197749585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32697887-C-G

197749585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32697887-C-T

http://identifiers.org/hco/3/GRCh38#197749704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32697990-C-A

197749704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32697990-C-T

197749726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32698009-G-T

http://identifiers.org/hco/3/GRCh38#197749728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28991
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#32698011-A-C