65658129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64827369-G-A

65658141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64827348-T-A

65658240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64827268-A-T

65658322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64827190-C-T

65658325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64827187-G-A

65658326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64827186-A-G

65658913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64826848-C-T

65659101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64826688-T-G

65659889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64826260-T-G

65659891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64826258-T-C

65660057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64826114-T-C

65660130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64826042-T-C

65660186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825964-A-G

65660186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825964-A-T

65660193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825957-C-T

65660242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825904-A-G

65660332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825828-T-G

65660334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825826-A-G

65660360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64825800-T-A

65660360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64825800-T-C

65660635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64825521-C-T

65660784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825373-T-G

65660789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64825368-C-T

http://identifiers.org/hco/15/GRCh38#65661065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64825113-C-A

65661429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64824783-T-C

65661499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64824704-T-G

http://identifiers.org/hco/15/GRCh38#65661543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64824660-C-A

65661573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64824633-C-T

65662037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64824193-G-A

65662037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64824193-G-T

65662061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64824169-A-G

http://identifiers.org/hco/15/GRCh38#65662249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64823969-C-A

65664308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64820042-A-G

65664412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64819938-T-G

65664429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64819921-T-C

http://identifiers.org/hco/15/GRCh38#65664504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64819849-C-A

65664504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64819849-C-T

65664548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64819808-A-T

65664590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64819766-A-G

65664617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64819739-C-T

65664662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64819694-A-G

65664685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64819671-A-G

65664731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64819625-G-A

65664756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64819601-T-C

65664809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64819551-T-C

http://identifiers.org/hco/15/GRCh38#65664816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64819544-C-A

65664825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64819535-T-C

http://identifiers.org/hco/15/GRCh38#65664836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64819524-C-A

65664836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64819524-C-T

65664887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64819466-A-G

http://identifiers.org/hco/15/GRCh38#65665005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64819353-A-C

65665333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64819074-G-T

65665550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64818489-G-T

65665574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64818467-G-A

65665574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64818467-G-C

65665766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64818280-C-T

65667021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64817583-C-T

65667391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64817523-T-A

65667391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64817523-T-C

65667414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64817500-A-T

http://identifiers.org/hco/15/GRCh38#65667732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64817188-C-A

65667752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64817173-G-T

http://identifiers.org/hco/15/GRCh38#65667754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64817171-C-A

http://identifiers.org/hco/15/GRCh38#65667850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64817051-C-A

65667850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64817051-C-T

65668031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64816873-G-A

65669273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64815958-G-A

http://identifiers.org/hco/15/GRCh38#65669287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64815943-A-C

65669509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64815326-T-G

http://identifiers.org/hco/15/GRCh38#65669716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64814571-C-A

65669716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64814571-C-T

65669937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64814371-A-G

65670004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64814302-T-C

65670004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64814302-T-G

http://identifiers.org/hco/15/GRCh38#65670013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64814293-C-A

http://identifiers.org/hco/15/GRCh38#65670257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64814052-A-C

65670981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64813775-T-G

65671076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64813725-C-T

65671758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64813408-G-A

65671758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64813408-G-T

65671829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64813338-G-A

65671829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64813338-G-C

65671829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64813338-G-T

65676294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64811757-G-A

65676306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64811745-T-C

http://identifiers.org/hco/15/GRCh38#65676325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64811708-C-A

65676368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64811668-A-G

65676792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64811286-A-T

65676812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64811266-A-T

65689875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64805461-C-T

65690030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64805311-C-T

http://identifiers.org/hco/15/GRCh38#65690369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64804752-A-C

65690369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64804752-A-G

65690375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64804746-G-T

65690381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64804740-G-T

65690656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64804469-G-A

65691232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64803893-G-T

65691305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64803820-G-C

65691407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64803718-T-C

65691414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: synonymous variant
orthologous variants: 64803711-G-A

65691564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64803562-G-A

65691564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64803562-G-T

65696577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64801599-T-C

65696785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64801400-A-G

http://identifiers.org/hco/15/GRCh38#65696792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64801392-A-C

65696792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64801392-A-G

65697231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64800721-T-C

65697239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64800713-A-G

65697603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64800169-A-T

http://identifiers.org/hco/15/GRCh38#65697684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64800091-C-A

65697684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64800091-C-G

65698586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64799376-A-T

65698606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64799356-T-G

65700064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64798587-G-A

65700127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64798525-T-C

65700496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64798136-A-G

65700500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64798132-T-C

65700658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64798038-C-T

65701029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64797047-G-A

65701029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64797047-G-C

65701616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64796763-A-G

65702381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense variant
orthologous variants: 64796330-G-A

65702514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 64796197-G-A

65702805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64795973-C-G

65702805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64795973-C-T

http://identifiers.org/hco/15/GRCh38#65703127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64795666-C-A

65703298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64795517-T-C

65703396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64795420-C-T

65703467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64795187-C-T

65703494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64795161-G-C

http://identifiers.org/hco/15/GRCh38#65705529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64794894-A-C

65705620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64794801-A-G

65705934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64794420-A-G

http://identifiers.org/hco/15/GRCh38#65706035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64794323-C-A

65706036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64794322-A-G

65706305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64794059-A-G

65706499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64793967-T-C

65706696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64793786-A-G

65708651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64785062-C-T

65708662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64785053-G-A

65709096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64784677-A-T

65709192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64784582-A-G

65709220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64784553-G-A

http://identifiers.org/hco/15/GRCh38#65709414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64784367-A-C

65709779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64784317-G-T

http://identifiers.org/hco/15/GRCh38#65710396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64783106-C-A

http://identifiers.org/hco/15/GRCh38#65710397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64783105-C-A

65710485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64783019-A-G

65714728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64781601-T-A

65714975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64781366-G-T

65715065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64781277-C-T

65715066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64781276-G-A

65715066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64781276-G-C

65715066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron variant
orthologous variants: 64781276-G-T

http://identifiers.org/hco/15/GRCh38#65715112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64781232-C-A

65715112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64781232-C-T

65715259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64780628-T-G

http://identifiers.org/hco/15/GRCh38#65715260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64780627-A-C

http://identifiers.org/hco/15/GRCh38#65715396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64780502-C-A

65715396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64780502-C-G

65715396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64780502-C-T

65715599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 64780298-G-T

http://identifiers.org/hco/15/GRCh38#65715608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64780289-C-A

65715608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64780289-C-T

65715626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64780271-G-T

http://identifiers.org/hco/15/GRCh38#65715738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64780176-C-A

65715738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64780176-C-T

65717121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779866-C-G

65717225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779800-T-C

65717598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779479-T-C

65717672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779432-T-C

65717819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64779285-G-T

http://identifiers.org/hco/15/GRCh38#65717972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64779132-C-A

65717972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64779132-C-G

http://identifiers.org/hco/15/GRCh38#65718006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64779098-C-A

65718006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779098-C-T

65718012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779092-G-A

65718012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779092-G-C

65718012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779092-G-T

65718013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779091-T-A

65718013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64779091-T-C

65718161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64778941-T-A

65720982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64776939-T-C

http://identifiers.org/hco/15/GRCh38#65721043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64776863-A-C

65721076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64776826-G-T

65721102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64776799-C-T

65721107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64776794-C-T

65722775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64775210-T-C

http://identifiers.org/hco/15/GRCh38#65722809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64775181-C-A

65722809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64775181-C-T

65722852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64775138-T-C

65723041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64774960-A-T

65723253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64774745-T-C

65723332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64774671-T-C

65723412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64774598-C-T

65724918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64773852-T-A

65725354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64773516-G-T

65725895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64773098-T-G

http://identifiers.org/hco/15/GRCh38#65726053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64772942-C-A

65726151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64772860-A-G

http://identifiers.org/hco/15/GRCh38#65726249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64772762-C-A

65726426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64771401-T-C

65726473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64771354-T-A

65726473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64771354-T-C

65726539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64770968-T-A

65726675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64770825-A-G

65728360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64770353-T-G

65728840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64770010-T-C

http://identifiers.org/hco/15/GRCh38#65729290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64769566-C-A

65729290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769566-C-G

65729290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769566-C-T

http://identifiers.org/hco/15/GRCh38#65729306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64769550-C-A

65729306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769550-C-T

65729323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769533-T-C

65729392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769463-T-C

65729814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769104-T-A

65729814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769104-T-C

65729849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64769069-G-A

65730362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64768254-G-A

65730788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767767-G-A

65730803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767752-T-C

65731341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767109-G-A

65731341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767109-G-T

65731417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767059-A-G

http://identifiers.org/hco/15/GRCh38#65731439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64767038-C-A

65731439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767038-C-G

65731439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64767038-C-T

65731527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766953-G-C

65731527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766953-G-T

65731580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766900-T-C

65731617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766662-T-C

65731775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766514-A-G

65731776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766513-T-C

http://identifiers.org/hco/15/GRCh38#65731813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64766482-C-A

http://identifiers.org/hco/15/GRCh38#65731833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64766465-C-A

65731833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766465-C-T

65732076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64766246-G-A

http://identifiers.org/hco/15/GRCh38#65732328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64766015-A-C

65732719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64765041-T-A

65732719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64765041-T-C

65732742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64765023-A-G

65732774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64764991-T-C

65732853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64764910-G-T

http://identifiers.org/hco/15/GRCh38#65732877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64764844-C-A

65732877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64764844-C-G

http://identifiers.org/hco/15/GRCh38#65732892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64764829-A-C

65732892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64764829-A-G

65732899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64764803-G-C

65732899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64764803-G-T

65732908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64764728-A-T

65733524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64763800-C-G

65734720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64763622-A-G

65737550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64760389-A-G

http://identifiers.org/hco/15/GRCh38#65737622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64760308-A-C

65737639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64760291-T-C

65737639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64760291-T-G

65737776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64759868-G-A

65737776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64759868-G-C

65737776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64759868-G-T

65737984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759658-A-G

65737984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759658-A-T

http://identifiers.org/hco/15/GRCh38#65738025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64759617-A-C

65738033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759609-T-A

65738157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759356-G-C

65738372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759074-G-C

65738372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759074-G-T

65738373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64759073-T-C

65738477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758885-A-T

65738656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758717-T-C

65738656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758717-T-G

65738857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64758510-G-T

65738992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758375-T-C

65739020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758348-T-C

65739119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758250-A-T

65739148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64758220-C-G

65739531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64757815-T-C

65739650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64757218-G-A

65741597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756614-T-C

65741634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756554-T-C

65741634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756554-T-G

65741690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756501-G-A

65741690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756501-G-C

http://identifiers.org/hco/15/GRCh38#65741703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64756487-A-C

65741704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756486-A-G

65741771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64756419-A-G

65741812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756381-T-C

65741845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756348-G-A

65741845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756348-G-C

65741845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756348-G-T

65741861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756332-T-C

65741912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64756282-T-C

http://identifiers.org/hco/15/GRCh38#65751883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64750465-A-C

65751891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750457-G-A

65751966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750357-G-A

65752105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750229-T-C

http://identifiers.org/hco/15/GRCh38#65752252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64750068-C-A

65752252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750068-C-G

65752252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750068-C-T

http://identifiers.org/hco/15/GRCh38#65752266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64750057-A-C

65752266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750057-A-T

65752327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750026-T-A

65752327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750026-T-C

65752327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64750026-T-G

65752434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64749914-C-T

65752474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 64749874-A-G

65752643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64749704-T-A

65754592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747967-T-C

65754670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747892-C-G

65754705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747857-A-G

65754738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747823-C-T

http://identifiers.org/hco/15/GRCh38#65754765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64747796-C-A

65754777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747784-T-C

65755120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747441-C-T

65755154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747405-T-C

65755160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747401-G-C

65755308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64747243-T-G

65755636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746970-T-C

65755648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746958-C-G

65755651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746955-A-G

65755877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746794-T-C

65755935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746741-C-G

65756109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746442-A-G

65756230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64746334-G-A

65756230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 64746334-G-C

http://identifiers.org/hco/15/GRCh38#65756503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64746065-C-A

65756503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746065-C-T

65756590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746009-G-A

65756590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746009-G-T

65756591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746008-T-A

65756591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746008-T-C

65756599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64746000-T-C

http://identifiers.org/hco/15/GRCh38#65756735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64745877-C-A

http://identifiers.org/hco/15/GRCh38#65758675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64745091-A-C

65758675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64745091-A-G

65758675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64745091-A-T

65758977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64744740-C-T

65761715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64742384-A-G

http://identifiers.org/hco/15/GRCh38#65761819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64742282-A-C

65763799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64740646-T-C

65763801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64740644-G-A

65763801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64740644-G-T

65763960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64740474-A-T

65764002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64740432-C-T

65764131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64740315-A-G

65766108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64739555-G-A

65766121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64739542-C-T

65766232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64739443-C-T

65766263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64739411-A-G

65766332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64739333-G-A

http://identifiers.org/hco/15/GRCh38#65766678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64739015-C-A

65766778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 64738917-T-A

65766778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 64738917-T-C

65766903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738805-T-C

65767140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738575-G-A

65767140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738575-G-T

65767158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738557-A-G

65767196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738520-G-C

65767210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738506-G-C

65767238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64738476-T-C

65769108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64733159-C-T

65769159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64733112-T-A

65769288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64733036-T-C

65769290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64733034-T-A

65769290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64733034-T-C

http://identifiers.org/hco/15/GRCh38#65769527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64732897-A-C

65769542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64732883-G-A

65772742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64732539-G-A

65772742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64732539-G-T

http://identifiers.org/hco/15/GRCh38#65772803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64732485-C-A

65772876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64732416-G-A

65773415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731955-T-G

http://identifiers.org/hco/15/GRCh38#65773502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64731875-C-A

65773502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731875-C-T

65773583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731819-T-C

65775650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731132-A-T

65775663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731119-A-G

65775663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731119-A-T

65775664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731118-G-A

65775664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731118-G-C

65775664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64731118-G-T

http://identifiers.org/hco/15/GRCh38#65775827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64731002-A-C

65775895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64730941-C-T

65776016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64730837-T-G

65776073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64730785-T-C

65778242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728885-A-G

65778297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728829-G-A

65778313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728808-C-T

65778340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728781-C-T

65778417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728707-T-A

65778417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728707-T-C

http://identifiers.org/hco/15/GRCh38#65778429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64728695-C-A

65778429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64728695-C-G

65780516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64727836-A-G

65780652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64727689-T-C

65781383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64726131-G-A

65781441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64726084-T-G

65785658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64722595-A-G

65785688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64722621-T-C

65786133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64724147-G-A

65786328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64723994-T-C

65787046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64722595-T-C

65787528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64722092-C-T

65787656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64721975-C-T

65787706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64721924-G-C

65787966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64721671-C-T

65788045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64721602-A-T

65788049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64721598-T-C

65789399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64721191-A-T

65789480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64721121-G-A

65790126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64720681-T-C

65790262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64720560-T-C

65790839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64720042-A-G

http://identifiers.org/hco/15/GRCh38#65791117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#64719758-C-A

65791139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64719734-G-C

65791447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64719390-T-C

http://identifiers.org/hco/15/GRCh38#65791451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#64719386-C-A

65791535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64719294-G-C

65791751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64719099-T-A

65791751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64719099-T-G

65791823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64719027-G-A

65791823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64719027-G-C

65791919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64718960-C-T

http://identifiers.org/hco/15/GRCh38#65791963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#64718914-A-C

65792058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 64718818-G-A

65792185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64718719-G-C

65792185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64718719-G-T

65792272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24321
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64718632-C-T