http://identifiers.org/hco/1/GRCh38#65248253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101351089-A-C

65248259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: non coding transcript exon variant
orthologous variants: 101351165-C-T

65248385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101351328-G-T

65248409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101351352-A-G

65248423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101351365-T-A

65248423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101351365-T-C

65249793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101351811-C-T

http://identifiers.org/hco/1/GRCh38#65249929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101351910-C-A

http://identifiers.org/hco/1/GRCh38#65254255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101353596-A-C

65254318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101353659-G-A

65254318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101353659-G-C

65254318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101353659-G-T

65254437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101353763-T-C

65254437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101353763-T-G

65254440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101353766-C-T

http://identifiers.org/hco/1/GRCh38#65254472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#101353797-C-A

65254472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101353797-C-T

65254497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101353821-G-A

65254497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101353821-G-T

65254528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101353848-C-G

65254528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101353848-C-T

65254547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 101353867-G-T

65254552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101353872-G-A

65254552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 101353872-G-T

65254570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 101353890-G-A

65254570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 101353890-G-T

http://identifiers.org/hco/1/GRCh38#65254622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#101353942-C-A

65254622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 101353942-C-T

http://identifiers.org/hco/1/GRCh38#65254685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#101353995-C-A

65254711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354024-G-A

65254711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354024-G-T

http://identifiers.org/hco/1/GRCh38#65254714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354027-C-A

65254714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354027-C-G

65254714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354027-C-T

http://identifiers.org/hco/1/GRCh38#65254717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354030-C-A

65254717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354030-C-T

http://identifiers.org/hco/1/GRCh38#65254787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354053-C-A

65254787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354053-C-T

65254818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354067-A-G

http://identifiers.org/hco/1/GRCh38#65254822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354071-C-A

65254822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354071-C-G

65254822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354071-C-T

65254829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101354078-T-A

65254829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101354078-T-C

http://identifiers.org/hco/1/GRCh38#65254846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354093-C-A

65254846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354093-C-T

65254849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354096-T-C

http://identifiers.org/hco/1/GRCh38#65254861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354108-C-A

65254861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354108-C-G

65254861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354108-C-T

http://identifiers.org/hco/1/GRCh38#65254864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354111-C-A

65254864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354111-C-T

65255120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354390-A-G

65255189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354463-C-T

http://identifiers.org/hco/1/GRCh38#65255193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101354467-C-A

65255335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101354574-A-T

65255885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355046-T-C

65255915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101355085-T-A

65256179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355341-A-G

65256360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355519-C-T

65256452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355636-C-T

65256506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355681-G-A

65256506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355681-G-C

65256574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101355735-T-C

http://identifiers.org/hco/1/GRCh38#65257422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101356202-C-A

65257614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101356382-A-G

65257852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101356628-T-C

65258093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101356822-T-C

65258094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101356823-T-C

65258540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101357172-A-G

65258588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101357216-G-A

65258588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101357216-G-T

65259062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101357941-C-T

65259154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358038-G-A

65259165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358049-C-G

65259165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358049-C-T

65259206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358087-C-T

http://identifiers.org/hco/1/GRCh38#65259265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101358126-A-C

65259506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358372-T-G

65259609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358632-T-C

http://identifiers.org/hco/1/GRCh38#65259638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101358661-C-A

65259676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358693-C-T

65259745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358733-T-C

65259771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358758-G-A

65259986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358942-C-G

65259986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101358942-C-T

65260106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101359026-G-C

65260150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101359069-G-A

65260535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101360099-A-G

65260542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101360111-A-G

http://identifiers.org/hco/1/GRCh38#65260564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101360133-C-A

65261357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101360563-G-C

65261364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101360570-T-C

65262972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101362061-T-C

65263183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101362822-T-C

65263707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101363318-G-A

http://identifiers.org/hco/1/GRCh38#65264065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101364496-A-C

65264098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101364529-A-G

http://identifiers.org/hco/1/GRCh38#65264130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101364561-A-C

65264141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101364575-G-T

65264245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101364680-A-T

65264440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101364864-T-G

65264519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101364955-C-T

65265005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101365433-T-C

http://identifiers.org/hco/1/GRCh38#65265007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101365435-C-A

65265007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101365435-C-T

65265368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101365782-C-T

65265392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101365806-A-G

65265580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366019-C-T

65265713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366102-T-C

65266266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366462-T-A

65266266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366462-T-C

65266266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366462-T-G

65266271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366467-A-G

65266457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366657-A-G

65266648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101366838-A-G

65267351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101367171-A-G

65267494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101367303-G-A

65267998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101367781-C-G

65268473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101368252-T-C

65268527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101368330-A-G

65268770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101368710-T-C

65269586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101369284-T-G

65269628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101369349-G-T

http://identifiers.org/hco/1/GRCh38#65278552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101373409-C-A

65278702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101373680-C-T

65278907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101373834-A-T

65278919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101373846-C-T

65279217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374171-A-G

65279246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374200-G-A

http://identifiers.org/hco/1/GRCh38#65279323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101374344-C-A

65279352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374389-G-A

65279352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374389-G-C

65279375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374415-G-A

65279375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374415-G-T

http://identifiers.org/hco/1/GRCh38#65279388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101374429-C-A

65279388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374429-C-T

65279440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101374470-A-G

65279571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101374619-A-G

65280220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101375960-A-T

65280232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101375975-G-A

65282305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101377148-G-A

65282669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101377428-T-C

65282708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101377464-T-C

http://identifiers.org/hco/1/GRCh38#65282773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101377527-A-C

65282773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101377527-A-G

65282812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101377564-A-G

65282858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101377610-T-C

65283193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101378593-G-A

65283318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101378723-T-C

65283693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379064-A-G

http://identifiers.org/hco/1/GRCh38#65283726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101379312-C-A

65283882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379464-C-T

65283940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379522-C-T

65284078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379615-C-T

65284091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379622-A-G

65284114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379651-G-C

65284168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379705-C-T

65284177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379714-A-G

65284184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379718-T-C

65284186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379720-A-G

65284251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379787-C-T

65284271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379807-T-C

65284271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379807-T-G

65284326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379882-T-C

65284348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101379904-T-C

65286682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101380105-G-A

65286682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101380105-G-T

65286800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101380215-A-G

65286987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382245-G-A

65287068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382307-C-T

65287081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382319-C-G

65287126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382363-G-A

65287180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382416-A-G

65287201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382437-G-T

65287414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101382640-T-G

http://identifiers.org/hco/1/GRCh38#65287550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101382876-A-C

http://identifiers.org/hco/1/GRCh38#65291933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101389964-C-A

65291933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101389964-C-T

65291971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101390021-G-A

65292112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101390144-G-A

http://identifiers.org/hco/1/GRCh38#65292357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101390448-C-A

65292357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101390448-C-T

65292409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101390499-G-T

65294581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101393242-A-G

65294738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101393390-T-C

65294929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101394000-A-G

65295008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101394079-T-C

65295333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101394370-T-C

65295448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101394458-G-A

65295609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395328-G-A

65295702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395418-T-C

65295715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395425-A-G

65295825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395514-T-C

65295850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395548-A-G

http://identifiers.org/hco/1/GRCh38#65295874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101395572-C-A

65295882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395579-T-C

65295887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395584-C-T

65295917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395614-A-G

65295917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395614-A-T

65296211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101395881-G-A

65296418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101396085-C-T

65296425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101396092-G-A

65296503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101396158-G-T

65298283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101398062-T-G

http://identifiers.org/hco/1/GRCh38#65299281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101398699-C-A

65299430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101398855-G-A

http://identifiers.org/hco/1/GRCh38#65299647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101399032-C-A

65303908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101400291-A-T

65304113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101400488-A-G

65304138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101400512-T-C

65304644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101401046-A-G

65305008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101401425-T-C

65305136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101401551-T-C

65305414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101402830-A-G

65305429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101402845-A-G

http://identifiers.org/hco/1/GRCh38#65307055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101405411-C-A

65307172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101405514-T-A

65307373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101405750-A-G

65307498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101405926-A-T

65307975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101406275-T-C

65307994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101406294-T-C

http://identifiers.org/hco/1/GRCh38#65308124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101406419-C-A

http://identifiers.org/hco/1/GRCh38#65308243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101406537-A-C

65308268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101406569-G-A

65308580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101406873-T-A

65308580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101406873-T-C

65308584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101406877-G-A

65308592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101406885-C-T

65309017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101407275-T-A

65309047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101407305-A-G

65309727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101407840-C-T

http://identifiers.org/hco/1/GRCh38#65309994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101408070-C-A

65309994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101408070-C-T

65311074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101409021-A-G

65311209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101409154-A-G

65311209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101409154-A-T

65312223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101409784-T-C

65312232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101409793-T-C

65312365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101409936-T-C

65312406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101409976-G-A

65312455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101410026-A-G

http://identifiers.org/hco/1/GRCh38#65312609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101410182-C-A

65312609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101410182-C-T

65312642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101410215-C-T

65312718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101410284-T-C

http://identifiers.org/hco/1/GRCh38#65312803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101410375-C-A

65312803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101410375-C-T

65313532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101410906-C-T

65313687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411058-A-G

65313711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411082-G-A

65313714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411085-A-G

65313884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411179-C-T

http://identifiers.org/hco/1/GRCh38#65313955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101411254-C-A

65313955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411254-C-T

65314089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411367-G-C

65314089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411367-G-T

65314203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101411696-T-C

http://identifiers.org/hco/1/GRCh38#65315307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101412912-C-A

65315307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101412912-C-T

65315483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101413341-A-G

65315930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101415550-T-C

65316077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101415715-G-A

65316465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101416063-C-T

http://identifiers.org/hco/1/GRCh38#65316528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#101416124-A-C

65316608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416190-G-A

65316639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416222-T-C

65316639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416222-T-G

65316737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416314-G-T

65316882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416445-G-A

65316896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416460-A-G

65317051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416702-G-A

65317238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416888-C-T

65317253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101416904-T-G

65317382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101417034-A-G

65317413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101417065-A-G

65317573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101417213-C-T

65317707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101417343-G-A

65319407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101417773-A-G

65319508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101417853-A-G

65320206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101418538-T-C

65321808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101419941-G-A

65321907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101420012-G-A

65322065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101420168-A-T

65322273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101420369-A-G

65322597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101420799-G-A

65322597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101420799-G-C

65322669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101420903-A-G

http://identifiers.org/hco/1/GRCh38#65322835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101421047-C-A

http://identifiers.org/hco/1/GRCh38#65324023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101421602-A-C

65324023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101421602-A-T

65324835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422110-T-A

65324867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422143-C-G

65325064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422316-T-C

65325130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422373-G-A

65325169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422412-G-A

65325169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422412-G-T

65325551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422581-T-C

65325667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101422688-G-T

65326746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101424148-G-C

65326810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101424202-C-T

65328360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425142-G-C

65328378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425160-A-T

65328388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425170-C-T

65328687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425482-G-A

http://identifiers.org/hco/1/GRCh38#65328721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101425516-C-A

65328721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425516-C-T

65328964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425698-G-A

65328964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425698-G-C

65328964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101425698-G-T

65329183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426167-T-C

65329340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426341-C-G

65329356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426357-T-G

65329670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426512-C-T

65329676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426518-C-T

65329690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426532-T-C

65329690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426532-T-G

65329712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426560-A-G

65329866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426652-C-T

65330228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101426973-C-T

http://identifiers.org/hco/1/GRCh38#65330443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101427153-A-C

http://identifiers.org/hco/1/GRCh38#65330788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101427176-A-C

65330986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427369-T-C

65331018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427391-C-T

65331190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427518-A-G

65331307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427624-G-A

65331442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427764-G-A

65331442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427764-G-T

65331446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427768-G-A

http://identifiers.org/hco/1/GRCh38#65331475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101427796-C-A

65331519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427840-G-A

65331587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101427901-T-C

65331893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101428410-T-C

65332206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101428738-A-G

65332219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101428751-G-T

65332527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429073-C-T

65332553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429100-A-G

65332569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429116-C-T

65332572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429118-G-C

65332715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429257-C-T

65333137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429652-T-C

65333348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429858-A-T

65333425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101429929-A-G

65334014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101430362-A-G

65339853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101436235-A-G

65340156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101436496-G-T

65340192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101436527-A-G

65340196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101436531-C-T

65340241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101436573-G-A

65340570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101437308-G-A

65340802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101437521-T-C

http://identifiers.org/hco/1/GRCh38#65340930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101437635-A-C

65341081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101438163-G-C

65341089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101438170-G-A

http://identifiers.org/hco/1/GRCh38#65341270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101438424-C-A

65341270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101438424-C-T

65341403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101438554-G-A

65341668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101438816-G-A

65341919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101439069-C-T

http://identifiers.org/hco/1/GRCh38#65342218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101439355-A-C

http://identifiers.org/hco/1/GRCh38#65342259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101439401-C-A

65342259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101439401-C-T

65342332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101439459-A-G

65342825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441018-T-C

65342881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441074-G-T

65342884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441077-A-G

65342902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441101-A-G

65343000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441192-T-G

65343264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441423-T-A

65343335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441486-T-G

65344147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441574-G-A

65344183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441610-G-A

65344410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101441827-G-T

65344860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442272-A-G

65345001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442369-C-T

65345002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442370-A-G

65345047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442415-A-G

65345122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442483-C-T

65345144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442504-C-T

65345188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101442557-C-T

http://identifiers.org/hco/1/GRCh38#65345664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101443049-A-C

65345681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101443066-A-T

http://identifiers.org/hco/1/GRCh38#65345709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101443094-C-A

65345709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101443094-C-G

65345709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101443094-C-T

65345725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101443110-T-G

http://identifiers.org/hco/1/GRCh38#65345785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101443148-C-A

65345785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101443148-C-T

http://identifiers.org/hco/1/GRCh38#65345786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101443149-C-A

65345793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101443156-G-A

http://identifiers.org/hco/1/GRCh38#65345835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101443201-C-A

65345841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101443207-C-T

http://identifiers.org/hco/1/GRCh38#65345870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101443234-C-A

65345870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101443234-C-T

65345941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101443302-C-T

65346064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101443604-C-T

65353435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101444753-G-T

65355636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101446078-T-C

65355761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101446198-A-G

65355806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101446228-G-A

http://identifiers.org/hco/1/GRCh38#65355860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101446268-A-C

65355990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101446441-C-G

65355993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101446444-C-T

http://identifiers.org/hco/1/GRCh38#65356007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101446463-A-C

65356660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101446787-A-T

http://identifiers.org/hco/1/GRCh38#65356790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101446898-A-C

65357060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447157-T-C

65357062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447159-A-G

65357105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447202-T-C

65357114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447211-C-T

65357253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447387-G-A

65357533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447616-C-T

65357544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447627-C-T

65357628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447650-A-T

65357673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101447677-G-C

http://identifiers.org/hco/1/GRCh38#65357806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101447791-C-A

65358779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101450116-T-A

65358779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101450116-T-C

65358784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101450121-C-T

65359159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101450862-T-C

65359159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101450862-T-G

65359310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451007-A-G

65359494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451206-G-T

65359535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451247-C-G

65359713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451351-G-A

65359713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451351-G-C

65359771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451406-G-A

65359843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101451527-A-G

65360342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101452065-C-T

65360590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101452289-G-T

65360630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101452329-C-T

65360644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101452342-G-A

http://identifiers.org/hco/1/GRCh38#65360667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101452365-A-C

65361192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454126-G-C

65361465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454365-A-G

65363833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454651-G-A

65363905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454722-A-G

65364489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454881-T-C

65364548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454934-A-G

65364566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454951-G-A

65364566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101454951-G-T

http://identifiers.org/hco/1/GRCh38#65364639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101455002-C-A

65364639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101455002-C-T

http://identifiers.org/hco/1/GRCh38#65364642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101455005-A-C

65364642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101455005-A-T

65364820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455182-C-T

65364821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455183-C-G

65364821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455183-C-T

65364836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455198-A-G

65364836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455198-A-T

http://identifiers.org/hco/1/GRCh38#65364865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101455227-C-A

65364865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455227-C-T

http://identifiers.org/hco/1/GRCh38#65364872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101455234-A-C

65364872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455234-A-G

65364981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455326-G-A

65365021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455366-C-T

65365042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455383-G-A

65365221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455525-A-G

http://identifiers.org/hco/1/GRCh38#65365222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101455526-A-C

http://identifiers.org/hco/1/GRCh38#65365371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101455666-C-A

65365375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455670-A-G

65365456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101455743-T-C

65365763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456034-G-A

65365763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456034-G-T

65365947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456210-T-C

65366004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456254-G-A

65366010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456256-A-G

http://identifiers.org/hco/1/GRCh38#65366067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101456311-C-A

65366067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101456311-C-T

65366233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456477-A-G

http://identifiers.org/hco/1/GRCh38#65366234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101456478-C-A

65366234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456478-C-T

http://identifiers.org/hco/1/GRCh38#65366287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101456553-A-C

65366287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456553-A-G

65366296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456561-T-C

65366333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456598-A-T

65366421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456679-C-T

65366589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456823-G-A

65366626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101456863-C-T

65369150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458110-A-G

65369213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458174-T-C

65369248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458210-C-T

65369274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458231-G-A

65369274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458231-G-T

65369478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458425-T-C

65369531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458476-T-G

65369795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458663-C-T

65369796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458664-G-A

65369892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101458749-G-A

65370408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101459489-C-T

65370517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101459581-C-T

65370534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101459597-G-A

65370683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101459739-G-A

65370796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101459850-T-G

65371023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460064-G-A

65371023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460064-G-T

65371027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460068-G-A

65371078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460111-A-G

65371162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460177-C-T

65371305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460302-C-T

http://identifiers.org/hco/1/GRCh38#65371595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101460994-A-C

65371599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460998-A-G

65371599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101460998-A-T

65371671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101461039-A-T

65371738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101461100-G-T

65371974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101461341-A-G

65371988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101461355-G-A

65372156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101461521-T-A

65372202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101461539-T-C

65377329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101462562-C-T

65379090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101463238-A-G

http://identifiers.org/hco/1/GRCh38#65379267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101463554-C-A

65379267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101463554-C-T

65379390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101463776-G-C

65379390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101463776-G-T

65379606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101463970-C-T

65379713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464298-T-A

65379717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464302-G-A

65379717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464302-G-T

65379730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464313-G-A

65379730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464313-G-T

65379750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464333-G-A

65379750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464333-G-T

65379782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101464365-A-G

http://identifiers.org/hco/1/GRCh38#65379814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101464396-C-A

65379814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464396-C-T

http://identifiers.org/hco/1/GRCh38#65379830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101464411-C-A

65379830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464411-C-T

65379846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464427-G-A

65379846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464427-G-T

65379913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464476-A-G

65380138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464706-G-T

65380244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464792-G-T

65380308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464858-A-G

65380444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464985-G-T

65380460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101464999-T-C

65383951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101468195-A-G

65383979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101468237-A-T

http://identifiers.org/hco/1/GRCh38#65384005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101468256-C-A

65384005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101468256-C-T

http://identifiers.org/hco/1/GRCh38#65384009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101468260-C-A

65384009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101468260-C-T

http://identifiers.org/hco/1/GRCh38#65384080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101468330-C-A

65384080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101468330-C-T

65384114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101468364-A-T

65384175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101468404-A-G

65384175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101468404-A-T

65384343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468572-G-A

65384343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468572-G-T

65384346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468575-G-A

65384346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468575-G-C

65384363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468592-G-A

http://identifiers.org/hco/1/GRCh38#65384376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101468605-C-A

65384377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468606-A-G

65384377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468606-A-T

65384385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468614-T-C

65384395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468624-G-T

65384408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468628-T-C

65384452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101468658-A-G

65385151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101469253-G-A

65385170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101469302-G-T

65385436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101469568-G-T

65385458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101469590-A-G

65385596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101469956-A-G

65385674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101470023-G-A

65386323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101470931-G-A

http://identifiers.org/hco/1/GRCh38#65386725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101471295-C-A

65386725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101471295-C-T

65386872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101471430-C-T

65387090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101471648-G-A

65387201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101471748-T-C

65387229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101471780-A-G

65387636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101472195-A-G

65387949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101472472-A-T

65388007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101472523-A-T

65388059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101472565-C-T

http://identifiers.org/hco/1/GRCh38#65388242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101472700-C-A

http://identifiers.org/hco/1/GRCh38#65388398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101472840-A-C

65388470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101472908-G-T

65388481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101472919-G-A

65388481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101472919-G-T

65389132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101473574-G-A

65389132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101473574-G-T

65389159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101473600-T-G

65389493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101473918-C-G

65389515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101473953-C-T

65389552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101473987-G-A

65389552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101473987-G-C

65389552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101473987-G-T

http://identifiers.org/hco/1/GRCh38#65389579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101474014-C-A

65389579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101474014-C-G

65389639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474072-T-C

65389642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474075-T-C

65389642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474075-T-G

65390145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474270-T-C

65390208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474332-T-A

65390376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474468-A-G

65390378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474471-T-C

65390493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474585-C-T

http://identifiers.org/hco/1/GRCh38#65390514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101474606-A-C

65390553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474645-C-G

65390553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474645-C-T

65390570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474662-C-T

65390590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474682-C-T

65390712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101474799-C-T

http://identifiers.org/hco/1/GRCh38#65390738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101474821-A-C

http://identifiers.org/hco/1/GRCh38#65392468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101475628-C-A

65392468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101475628-C-T

65392519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101475679-A-G

http://identifiers.org/hco/1/GRCh38#65392794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101475954-C-A

65392794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101475954-C-T

http://identifiers.org/hco/1/GRCh38#65392801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101475961-C-A

65392801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101475961-C-T

65392813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101475973-A-G

http://identifiers.org/hco/1/GRCh38#65392831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101475991-C-A

65392854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101476014-G-T

65392875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476034-T-C

http://identifiers.org/hco/1/GRCh38#65392912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101476068-C-A

65393022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476152-G-A

65393156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476788-A-G

65393158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476790-A-G

65393289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476920-C-T

65393319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476950-T-C

65393335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476966-G-A

65393366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101476997-G-A

65394073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101477666-A-G

65394139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101477735-G-A

65394211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101477810-G-A

65394211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101477810-G-T

65394411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101477987-C-G

65394803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101480686-G-C

65394803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101480686-G-T

65394812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101480695-G-T

65394824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101480707-G-A

65394878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101480838-A-G

65395041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481001-A-G

65395053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481013-G-T

http://identifiers.org/hco/1/GRCh38#65395058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101481018-C-A

65395058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481018-C-T

65395069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481035-A-G

65397685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481484-G-A

65397878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481677-A-T

65397934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101481739-G-C

http://identifiers.org/hco/1/GRCh38#65398327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101482435-C-A

65398355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482463-T-C

65398355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482463-T-G

65398515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482622-A-G

65398675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482762-A-G

65398713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482807-A-G

65398713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482807-A-T

65398775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482855-T-A

65398910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101482990-T-C

65398950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483031-T-C

65398951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483032-G-T

65398955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483036-A-G

65398955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483036-A-T

65398969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483048-G-T

http://identifiers.org/hco/1/GRCh38#65398978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101483056-C-A

65399074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483165-A-G

65399124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101483213-A-G

65401570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485043-C-G

http://identifiers.org/hco/1/GRCh38#65401610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101485083-C-A

65401610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485083-C-T

65401637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485110-A-T

http://identifiers.org/hco/1/GRCh38#65401682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101485155-C-A

65401682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485155-C-G

65401682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485155-C-T

65401727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485200-T-C

65401727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485200-T-G

65401737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485210-T-G

65401741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101485214-T-G

65401827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: 101485300-C-T

65404344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101490987-G-A

65404385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491028-G-A

65404385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491028-G-C

65404441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491084-T-G

65404581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491203-T-C

65404733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491348-G-C

65405331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491674-T-C

65405349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491691-C-T

65405449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491796-G-T

65405470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491807-T-A

65405603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491928-C-G

65405662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101491993-G-T

65405749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101492069-G-T

65405836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101492154-T-C

65405934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101492252-C-T

65406018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101492336-T-C

65406072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101492390-C-T

http://identifiers.org/hco/1/GRCh38#65406185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101492501-A-C

65407377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101492828-C-T

65407413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101492869-A-G

65407536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101492987-C-T

65407577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493032-G-C

http://identifiers.org/hco/1/GRCh38#65407638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101493094-A-C

65407817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493185-A-G

http://identifiers.org/hco/1/GRCh38#65407882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101493273-C-A

65407882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493273-C-T

65407917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493308-G-T

65407984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493357-A-T

65408077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, undefined
orthologous variants: 101493424-G-T

65408330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493645-G-C

http://identifiers.org/hco/1/GRCh38#65408384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101493697-A-C

http://identifiers.org/hco/1/GRCh38#65408503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101493831-C-A

65408539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493858-G-A

65408585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101493899-T-C

65408633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 101493947-T-C

65408841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101494135-G-A

http://identifiers.org/hco/1/GRCh38#65408887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101494178-C-A

65408887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101494178-C-T

65409128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101494423-G-A

65409274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101494622-T-C

65410664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101495830-T-C

65410761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101495924-G-A

65411178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496400-T-C

65411324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101496537-T-G

http://identifiers.org/hco/1/GRCh38#65411345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101496558-A-C

http://identifiers.org/hco/1/GRCh38#65411361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101496574-C-A

65411420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: synonymous variant
orthologous variants: 101496633-A-G

65411435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496648-A-G

http://identifiers.org/hco/1/GRCh38#65411497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101496716-C-A

65411509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496728-T-C

65411510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496729-G-A

65411510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496729-G-T

http://identifiers.org/hco/1/GRCh38#65411521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101496741-C-A

65411521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496741-C-G

65411521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496741-C-T

65411537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496757-T-A

65411537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496757-T-C

http://identifiers.org/hco/1/GRCh38#65411555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101496778-A-C

65411561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496784-T-C

65411591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496814-T-C

65412067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496920-C-T

65412112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496955-T-C

65412113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101496956-A-T

65412391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101497206-C-T

65412545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101497340-T-C

65412750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, undefined
orthologous variants: 101497517-T-C

65412755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron_variant, undefined
orthologous variants: 101497522-G-C

65412793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: intron variant
orthologous variants: 101497550-G-T

65413147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101497892-G-A

65413147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101497892-G-T

65413329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498054-G-A

65413525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498280-C-T

65413537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498292-G-T

65413568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498322-G-C

65413568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498322-G-T

65413596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498350-T-C

65413603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498357-A-T

65413644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498384-C-T

65413649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498389-A-G

65413659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498401-C-T

65414239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101498910-G-C

65414345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101499018-T-C

65414430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101499129-A-G

65414831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101499549-C-T

65414934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101499654-A-G

65414964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101499684-A-G

65415301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101500160-G-A

65415301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101500160-G-C

65415372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15469
most severe consequence: 3 prime UTR variant
orthologous variants: 101500325-A-G