92617479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426620-T-C

92617492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426607-T-C

92617492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426607-T-G

92617620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426479-C-T

92617652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426459-A-G

92617657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426454-T-C

http://identifiers.org/hco/15/GRCh38#92617736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73426377-C-A

92617736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426377-C-G

92617736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426377-C-T

92617764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426361-G-A

92617764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426361-G-T

http://identifiers.org/hco/15/GRCh38#92617770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73426355-C-A

92617775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426350-G-A

92617775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426350-G-T

92617778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426347-A-G

92617778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426347-A-T

http://identifiers.org/hco/15/GRCh38#92617782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73426343-C-A

92617782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426343-C-G

92617782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426343-C-T

92617828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426304-A-G

http://identifiers.org/hco/15/GRCh38#92617845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73426287-C-A

92617845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426287-C-T

92617877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426274-G-C

92617878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426273-G-A

92617878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426273-G-T

http://identifiers.org/hco/15/GRCh38#92618015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73426189-A-C

92618051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426148-T-G

92618072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426126-T-C

92618072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426126-T-G

92618103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73426097-G-A

92618124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426076-C-T

92618208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73426002-A-G

92618482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425790-A-G

92618541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425732-G-A

92618541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425732-G-T

http://identifiers.org/hco/15/GRCh38#92618559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73425702-C-A

http://identifiers.org/hco/15/GRCh38#92618587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73425673-A-C

92618587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425673-A-G

92618652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425611-T-A

92618652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425611-T-C

http://identifiers.org/hco/15/GRCh38#92618663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73425604-A-C

92618663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425604-A-G

92618664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425603-G-C

http://identifiers.org/hco/15/GRCh38#92618746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73425539-A-C

92618746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425539-A-G

http://identifiers.org/hco/15/GRCh38#92618747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73425538-C-A

92618747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425538-C-T

92618792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425498-T-A

92618792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425498-T-C

92618792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73425498-T-G

92619225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73424869-G-A

92619225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73424869-G-T

92619236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 73424858-G-A

92619236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 73424858-G-T

92619272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 73424821-A-G

92619276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 73424817-G-T

http://identifiers.org/hco/15/GRCh38#92619281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424812-C-A

92619281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 73424812-C-T

92619383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 73424716-G-T

http://identifiers.org/hco/15/GRCh38#92619544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424519-C-A

http://identifiers.org/hco/15/GRCh38#92619596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424456-C-A

92619596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424456-C-T

http://identifiers.org/hco/15/GRCh38#92619619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424433-C-A

92619619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424433-C-G

92619619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424433-C-T

http://identifiers.org/hco/15/GRCh38#92619640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424412-C-A

http://identifiers.org/hco/15/GRCh38#92619645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424407-C-A

92619645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424407-C-T

http://identifiers.org/hco/15/GRCh38#92619674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424378-C-A

92619674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424378-C-G

92619674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424378-C-T

http://identifiers.org/hco/15/GRCh38#92619683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424373-C-A

92619683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424373-C-G

92619683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73424373-C-T

http://identifiers.org/hco/15/GRCh38#92619820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424251-C-A

92619820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73424251-C-T

92619858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73424214-G-A

92619858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73424214-G-T

92619882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73424179-A-G

http://identifiers.org/hco/15/GRCh38#92619891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424170-C-A

92619891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73424170-C-T

http://identifiers.org/hco/15/GRCh38#92619956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73424128-C-A

92624504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422783-G-A

92624505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422782-G-A

92624569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422731-C-G

92624569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422731-C-T

92624622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422697-C-T

92624874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422454-C-G

92624874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422454-C-T

92624875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422453-G-A

92625074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422259-T-C

92625204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73422088-T-A

92625284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73422029-A-G

http://identifiers.org/hco/15/GRCh38#92625312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73422001-C-A

92625326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73421987-G-A

http://identifiers.org/hco/15/GRCh38#92625402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73421909-A-C

http://identifiers.org/hco/15/GRCh38#92625516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73421801-A-C

92625544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73421737-C-G

92625630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73421637-C-T

92626590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73419534-C-T

92626637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73419488-T-C

92626658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73419467-T-C

92627084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419374-A-G

http://identifiers.org/hco/15/GRCh38#92627116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73419342-C-A

92627117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419341-A-G

92627161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419315-A-T

92627182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419300-C-G

http://identifiers.org/hco/15/GRCh38#92627207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73419270-C-A

92627207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419270-C-T

92627327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419146-G-A

92627348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73419125-T-C

92628550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73416881-G-A

92630134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73416427-A-G

92630375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73416203-C-T

http://identifiers.org/hco/15/GRCh38#92630398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73416183-C-A

92630398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73416183-C-G

92630398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73416183-C-T

http://identifiers.org/hco/15/GRCh38#92630463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73416127-C-A

92630532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73416077-C-T

92632157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73415188-G-T

92633092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414922-T-C

http://identifiers.org/hco/15/GRCh38#92633129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73414885-A-C

92633129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414885-A-G

92633134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414880-G-A

92633174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414857-G-A

92633260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414777-T-C

92633291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414748-T-C

92633300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73414739-T-C

92633645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73412718-G-A

92635290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73411604-G-C

92635960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73411312-A-G

92636008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73411268-T-C

92636026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73411250-C-T

92636409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73410401-C-T

92636473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73410339-C-T

92636667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73410185-C-T

http://identifiers.org/hco/15/GRCh38#92636841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73409990-A-C

92636841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73409990-A-G

http://identifiers.org/hco/15/GRCh38#92636863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73409968-C-A

92636970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73409862-T-C

http://identifiers.org/hco/15/GRCh38#92637019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73409810-C-A

92637504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73409468-A-T

92638695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73405077-C-T

92641264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73404014-T-C

92641553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73403778-T-C

92641884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73403425-A-T

92643690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73400521-C-T

http://identifiers.org/hco/15/GRCh38#92643695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73400516-C-A

92643695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73400516-C-T

92643942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73400325-T-G

92644006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73400257-G-C

92644079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73400192-C-G

92644079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73400192-C-T

92644403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73399911-T-A

92644410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73399904-A-G

92644412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73399902-A-G

http://identifiers.org/hco/15/GRCh38#92644617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73399715-C-A

92644677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73399657-G-A

92644787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73399416-C-G

92644797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73399305-C-T

http://identifiers.org/hco/15/GRCh38#92644798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73399304-A-C

92644842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73399254-C-T

92645298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73398878-G-T

92645394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73398811-G-T

92645398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73398807-T-C

92645443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73398785-A-G

http://identifiers.org/hco/15/GRCh38#92645543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73398704-A-C

92645543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73398704-A-G

92645578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73398655-C-G

http://identifiers.org/hco/15/GRCh38#92645634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73398595-C-A

92645634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73398595-C-G

92645634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73398595-C-T

92645643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73398586-G-T

92645666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73398567-A-G

92645697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73398539-A-G

92645915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73398343-C-T

92647386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397731-T-C

92648374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397644-T-C

http://identifiers.org/hco/15/GRCh38#92648423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73397589-C-A

92648466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397544-T-C

92648788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397264-G-A

92648853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397200-T-C

92648853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397200-T-G

92648870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73397174-A-G

92649133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396951-C-T

92649162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396938-T-C

92649179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396921-C-G

92649194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396909-T-A

92649287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396815-A-G

92649347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396756-G-A

92649409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396732-C-T

92649414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396726-T-C

92649566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396576-A-G

92649591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396550-C-T

92649630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396510-C-T

92649688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73396456-T-A

92650513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73395871-G-C

92650513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73395871-G-T

92650540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73395845-G-A

92650540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73395845-G-C

92650623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73395776-C-T

92651785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73393514-G-A

92651785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73393514-G-C

92651811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73393472-C-T

92651983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73393310-T-G

92652009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73393256-G-A

92652011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73393254-A-G

http://identifiers.org/hco/15/GRCh38#92652175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73393088-A-C

http://identifiers.org/hco/15/GRCh38#92652197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73393078-C-A

http://identifiers.org/hco/15/GRCh38#92652805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73391811-C-A

92652813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391803-G-A

92652899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391717-G-A

92652899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391717-G-C

92652990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73391636-T-C

92653081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391582-C-T

92653091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391573-T-C

92653320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391365-G-A

92653320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391365-G-T

92653369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391316-T-C

92653480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391210-C-G

92653480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73391210-C-T

92655036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73390867-G-C

92655036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73390867-G-T

http://identifiers.org/hco/15/GRCh38#92655041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390862-C-A

92655041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73390862-C-G

92655041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73390862-C-T

http://identifiers.org/hco/15/GRCh38#92655151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390758-C-A

92655151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390758-C-G

92655151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390758-C-T

92655152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390757-A-G

92655152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390757-A-T

http://identifiers.org/hco/15/GRCh38#92655154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390755-C-A

92655154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390755-C-T

http://identifiers.org/hco/15/GRCh38#92655164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390745-C-A

92655164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390745-C-G

92655164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390745-C-T

92655189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390719-A-G

92655207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73390700-G-A

92655238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73390664-G-A

92655258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390632-A-G

92655262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390628-T-C

http://identifiers.org/hco/15/GRCh38#92655283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390607-C-A

92655283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73390607-C-T

92655296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73390594-A-G

http://identifiers.org/hco/15/GRCh38#92655297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390593-A-C

92655297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73390593-A-G

92655330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 73390560-C-T

92655443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 73390447-T-C

http://identifiers.org/hco/15/GRCh38#92655473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390426-C-A

92655473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 73390426-C-T

http://identifiers.org/hco/15/GRCh38#92655517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390388-C-A

92655517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: 73390388-C-G

92655517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: 73390388-C-T

92655547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: 73390364-T-C

http://identifiers.org/hco/15/GRCh38#92655618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73390293-C-A

92655618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73390293-C-G

92655618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73390293-C-T

92655646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: 73390262-G-A

92655646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: 73390262-G-C

92655646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, missense_variant
orthologous variants: 73390262-G-T

92655750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73390140-G-A

92655750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73390140-G-T

92655885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, undefined
orthologous variants: 73390008-A-G

92655926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389970-C-T

92656208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389764-T-C

http://identifiers.org/hco/15/GRCh38#92656415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73389662-C-A

92656415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389662-C-T

92656481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389605-A-G

92656545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73389555-A-G

92656589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73389535-G-C

92656639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389491-G-A

92656646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389484-G-A

92656646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389484-G-T

92656647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389483-G-T

92656715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389417-T-C

http://identifiers.org/hco/15/GRCh38#92656791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73389365-C-A

92656791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389365-C-T

92656870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389287-T-G

92656902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389255-G-A

92657110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389057-T-A

92657110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389057-T-G

92657152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73389015-T-C

92657252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73388915-G-A

92657675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73388413-C-T

92658340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73387853-G-T

92658486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73387571-G-A

92661256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371690-G-A

92661333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371616-G-A

92661333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371616-G-T

92661347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371599-C-G

92661347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371599-C-T

http://identifiers.org/hco/15/GRCh38#92661371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73371567-A-C

92661443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371500-T-C

92662148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73371055-T-C

92662353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73370857-T-C

92662825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73370715-T-A

92665336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73368395-C-G

92665428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73368307-C-G

92665540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73368195-A-G

92665656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73368078-C-G

92665656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73368078-C-T

92665745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73367989-T-C

92665759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73367974-C-G

92666657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73367074-A-T

92666697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73367035-T-C

http://identifiers.org/hco/15/GRCh38#92666729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73367009-A-C

92667099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73366281-G-A

http://identifiers.org/hco/15/GRCh38#92667158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73366220-C-A

92667240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73366136-T-C

92667251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73366125-G-C

92667705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73365658-C-T

92667757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73365637-G-A

92667757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73365637-G-T

92670784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73362275-G-C

92671878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73359404-A-G

92671935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: -T-C

92671935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: -T-G

92672014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: -A-T

92673078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73353696-A-T

http://identifiers.org/hco/15/GRCh38#92673288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73353496-A-C

92673288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73353496-A-T

92673333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73353448-T-C

92681342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73350400-A-G

92681435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73350310-T-C

92681481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, undefined
orthologous variants: 73350264-T-C

92681549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, undefined
orthologous variants: 73350193-C-T

92681721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73348666-T-C

92682218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73348300-T-A

92682218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73348300-T-C

http://identifiers.org/hco/15/GRCh38#92687194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73345250-A-C

92687488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73344969-G-C

92687559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73344897-T-C

92687711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73344760-A-G

92690216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343748-A-G

92690280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343694-G-A

92690441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343562-A-G

92690688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343312-G-A

92690700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343300-T-G

http://identifiers.org/hco/15/GRCh38#92690809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73343191-A-C

92690955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343038-G-A

92690983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73343011-C-G

92691072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73342918-C-T

92691851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73342284-G-A

92691851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73342284-G-C

92692122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73342073-A-T

92692137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73342058-G-A

92693397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341619-C-G

92693506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341527-T-C

92693506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341527-T-G

92693601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341417-C-G

92693691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341360-C-G

92693728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341327-T-C

92693729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73341326-T-G

92695410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73340733-T-A

92695410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73340733-T-C

http://identifiers.org/hco/15/GRCh38#92695430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73340713-A-C

92695456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73340688-T-C

92695569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73340574-T-A

92695569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73340574-T-C

92695807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73340350-T-C

92696177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73332772-A-G

92696234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73332711-G-C

92696244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73332701-T-C

92696312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73332642-A-G

92696432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73332527-A-G

92696736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73331918-G-C

92696823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73331829-T-C

92696823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73331829-T-G

92696840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73331812-A-G

92696872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73331781-G-C

92696983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73331655-T-C

92701935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73315783-A-G

92702010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73315686-T-A

92702067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73315629-G-A

92702067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73315629-G-T

92702077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73315621-G-A

92702114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73315584-G-C

92704209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73314982-G-A

92704479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73314745-A-G

92704507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73314715-T-C

92704536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73314685-C-T

http://identifiers.org/hco/15/GRCh38#92704591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73314634-C-A

92704591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73314634-C-T

92705373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312889-T-A

92705373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312889-T-C

92705580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312692-T-C

http://identifiers.org/hco/15/GRCh38#92705617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73312659-A-C

92705662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312616-G-A

92705676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312602-T-C

92705680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312598-A-G

92705729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312548-C-T

92705803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312481-A-G

92705862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312411-A-G

92705863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73312410-T-C

http://identifiers.org/hco/15/GRCh38#92706318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73311182-A-C

92706605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73310722-G-A

92706605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73310722-G-C

92706628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73310698-G-C

92706821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73310091-A-G

92706948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309969-G-A

http://identifiers.org/hco/15/GRCh38#92707216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73309711-A-C

92707216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309711-A-G

92707315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309615-G-A

92707727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309225-G-T

92707798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309102-C-T

92707806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309094-T-A

92707806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73309094-T-C

92708024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73308854-G-A

92708024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73308854-G-T

http://identifiers.org/hco/15/GRCh38#92708112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73308764-C-A

92708147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73308730-G-T

92708276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73308165-T-C

92708297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73308144-G-A

92708804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307691-C-T

92708889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307620-T-A

http://identifiers.org/hco/15/GRCh38#92708965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73307555-C-A

92709000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307510-G-A

92709029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307436-G-A

92709112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307370-T-C

http://identifiers.org/hco/15/GRCh38#92709179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73307317-C-A

92709223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307264-G-C

92709238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307261-C-T

92709239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307260-A-G

92709254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307245-G-A

92709258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307241-T-C

92709298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73307202-T-C

92715010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73305709-C-G

92715660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73305172-C-T

http://identifiers.org/hco/15/GRCh38#92715772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73305061-C-A

92715815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73305021-C-T

92715900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73304932-G-A

92715900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73304932-G-T

http://identifiers.org/hco/15/GRCh38#92715931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73304908-C-A

92715933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73304906-G-T

92715948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73304891-G-A

92715948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73304891-G-T

92715958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73304881-A-G

http://identifiers.org/hco/15/GRCh38#92716033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73304807-C-A

92716056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73304785-G-C

92716056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73304785-G-T

92716300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304709-G-A

92716300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304709-G-C

92716300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304709-G-T

92716364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304633-A-G

92716378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304614-A-G

92716449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304544-C-T

92716543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304448-A-G

92716544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304447-G-T

92716549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304442-T-G

92716596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304400-C-T

92716885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304166-C-T

92716983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73304068-C-G

92742955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73294733-T-G

92742977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73294708-C-G

http://identifiers.org/hco/15/GRCh38#92743252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73294266-C-A

92743252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73294266-C-T

92743269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73294249-C-T

92743690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73293810-C-G

http://identifiers.org/hco/15/GRCh38#92743772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73293724-A-C

92743791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron variant
orthologous variants: 73293702-G-A

92780704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73287928-T-C

92780984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73287625-T-C

92787943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73283023-A-G

92788147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73280957-C-T

92788226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73280892-G-T

92789557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73280721-T-C

92789557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73280721-T-G

92789590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 73280688-G-C

92790000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73280596-C-T

92790108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73280484-T-C

92794552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73278481-G-A

92794895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73278444-A-G

92797454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73278011-C-T

92797626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73277869-T-C

92797768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73277736-A-G

92801545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73274172-T-C

92801548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73274169-T-C

92809173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268356-G-A

92809173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268356-G-T

92809201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268328-A-G

92809353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268181-G-T

http://identifiers.org/hco/15/GRCh38#92809426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73268068-C-A

92809426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268068-C-T

92809447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268047-C-T

92809469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73268026-G-A

http://identifiers.org/hco/15/GRCh38#92809475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73268020-C-A

92809489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73267995-T-A

http://identifiers.org/hco/15/GRCh38#92809497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#73267987-C-A

92809497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73267987-C-G

92809505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73267979-T-C

http://identifiers.org/hco/15/GRCh38#92809511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73267973-C-A

92809511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73267973-C-T

92809535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73267954-G-A

92809554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73267933-G-A

http://identifiers.org/hco/15/GRCh38#92809610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73267890-C-A

92809610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73267890-C-G

92809662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 73267869-C-G

http://identifiers.org/hco/15/GRCh38#92809686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34339
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#73267843-C-A