64759508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 121200923-C-T

64759530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121200907-T-C

64759530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121200907-T-G

64780224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121187450-T-C

64780755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121187301-G-A

64780760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121187296-C-G

64780760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121187296-C-T

64780761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121187295-G-A

64780761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121187295-G-T

64780993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 121187201-A-G

64780993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 121187201-A-T

64781088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 121187118-G-A

64781088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 121187118-G-T

64781105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187101-G-A

64781105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187101-G-C

64781105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187101-G-T

http://identifiers.org/hco/12/GRCh38#64781117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121187086-C-A

64781117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187086-C-T

64781120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187083-G-A

64781120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187083-G-T

http://identifiers.org/hco/12/GRCh38#64781130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121187073-C-A

64781130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 121187073-C-T

64781135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 121187068-G-T

64781160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 121187043-T-C

64781163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 121187040-A-G

http://identifiers.org/hco/12/GRCh38#64781244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121186962-C-A

64781244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121186962-C-G

64781244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 121186962-C-T

64782053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121186176-G-C

64782177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121186060-A-G

64783256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121185130-A-T

64783277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121185110-C-T

64783521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121184930-T-A

64783521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121184930-T-C

64785646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121183403-C-T

64785696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121183351-G-C

http://identifiers.org/hco/12/GRCh38#64785747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121183296-C-A

64785899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121183154-C-T

64785913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121183140-C-T

http://identifiers.org/hco/12/GRCh38#64786188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121182892-C-A

http://identifiers.org/hco/12/GRCh38#64786193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121182887-A-C

64786193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121182887-A-G

http://identifiers.org/hco/12/GRCh38#64787511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121182248-A-C

64788005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121182041-G-C

64788270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121181882-G-C

64788539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121181656-T-C

http://identifiers.org/hco/12/GRCh38#64789875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121180289-C-A

64790027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121180160-A-T

64790485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121178936-A-G

64790557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121178859-A-T

64790580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121178836-T-C

64790661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121178758-C-G

64790661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121178758-C-T

64790663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121178756-C-G

64792161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121176135-G-T

64792335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121175979-C-T

http://identifiers.org/hco/12/GRCh38#64792894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121172488-C-A

64795791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171311-G-T

http://identifiers.org/hco/12/GRCh38#64795827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121171276-C-A

64795827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171276-C-T

64795840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171263-A-G

64795840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171263-A-T

64795908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171239-G-A

64795982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171169-C-T

64796024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171141-A-G

64796141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121171018-G-T

64796416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121170690-T-C

64796496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121170608-A-G

64796508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121170596-C-T

64797080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121169968-C-T

64797380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121169590-G-T

64797414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121169556-G-A

64797483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121169497-T-C

64797513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121169468-T-C

64797555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121169433-G-A

64801801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121167688-G-A

64801802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121167687-G-A

64805575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121165966-G-A

64805575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121165966-G-C

64805625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121165923-G-A

http://identifiers.org/hco/12/GRCh38#64805674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121165877-A-C

64806225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121165661-A-T

64811298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121163795-A-G

64811538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121163565-T-A

64811544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121163559-G-A

64811552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121163551-G-C

http://identifiers.org/hco/12/GRCh38#64811589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121163506-C-A

64811591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121163504-C-T

64811944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121163165-A-T

http://identifiers.org/hco/12/GRCh38#64812130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121162666-C-A

64812354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121162451-T-C

64812630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121161925-T-A

64812640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121161915-A-G

64812704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121161852-G-C

64813127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121161466-A-G

64813437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121161167-G-T

64813766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121160878-A-G

64813811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121160835-A-G

64814027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121160612-A-G

64814373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121160570-A-G

64814693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121159531-T-A

http://identifiers.org/hco/12/GRCh38#64814800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121159426-A-C

64814810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121159416-C-T

64816380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121156976-A-G

64816413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121156938-T-A

64816698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121156708-C-T

64819213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152547-G-A

64819295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152454-C-T

64819368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152381-C-T

64819391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152352-G-T

http://identifiers.org/hco/12/GRCh38#64819401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121152342-A-C

http://identifiers.org/hco/12/GRCh38#64819444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121152277-C-A

64819444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152277-C-G

64819444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152277-C-T

64819476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152241-G-T

64819485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152195-C-T

64819518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152167-G-A

64819564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121152105-G-A

64819808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121151909-C-T

http://identifiers.org/hco/12/GRCh38#64820203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121151445-C-A

64821210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121150440-G-A

64821221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121150429-G-A

64821667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121150050-C-T

64821770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121149974-C-T

64821811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121149934-C-G

64824265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121147277-A-G

64824445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121147098-T-C

http://identifiers.org/hco/12/GRCh38#64824700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121146867-C-A

64824700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146867-C-T

64825037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146543-A-G

64825156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146504-G-T

64825272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146422-T-A

64825272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146422-T-C

64825272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146422-T-G

64825338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121146359-G-A

64825338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121146359-G-C

64825338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121146359-G-T

64825403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146294-T-G

http://identifiers.org/hco/12/GRCh38#64825526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121146183-C-A

64825526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146183-C-T

64825528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146181-G-A

64825528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146181-G-T

64825529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146180-G-T

64825530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146179-G-A

64825530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146179-G-C

64825530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146179-G-T

http://identifiers.org/hco/12/GRCh38#64825549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121146177-C-A

http://identifiers.org/hco/12/GRCh38#64825576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121146152-C-A

64825576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146152-C-T

64825620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146107-G-A

http://identifiers.org/hco/12/GRCh38#64825644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121146083-A-C

64825644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146083-A-G

64825703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146032-C-G

64825703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121146032-C-T

64825781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121145954-G-C

64825883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121145856-G-C

64826164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121145569-C-G

64826423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121145313-G-A

64826488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121145244-T-C

64826541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121145198-C-T

64826557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121145185-G-C

64826557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121145185-G-T

64826565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121145176-G-T

64826914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121144823-A-G

http://identifiers.org/hco/12/GRCh38#64827694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121142910-C-A

64827694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142910-C-G

64827694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142910-C-T

64827730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142883-A-T

64827751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142862-G-T

64827793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142824-T-G

64828402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142165-G-T

http://identifiers.org/hco/12/GRCh38#64828414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121142153-C-A

64828414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142153-C-T

http://identifiers.org/hco/12/GRCh38#64828529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121142038-C-A

64828529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142038-C-T

64828547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142020-A-G

64828547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121142020-A-T

http://identifiers.org/hco/12/GRCh38#64828555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121142013-C-A

64828591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141977-T-A

64828591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141977-T-G

http://identifiers.org/hco/12/GRCh38#64828618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121141973-C-A

64828618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141973-C-G

64828682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141921-C-T

64828765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141826-T-C

64828885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141724-C-T

64828894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141715-G-A

64828894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141715-G-T

64829074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141598-A-G

64829083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141589-A-G

64829382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141343-C-G

64829509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141201-C-T

64829657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121141023-A-G

64829966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140739-A-G

64830088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140630-A-G

64830097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140619-G-A

64830210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140516-T-C

http://identifiers.org/hco/12/GRCh38#64830213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121140513-A-C

64830294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140451-G-T

64830326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140419-G-A

64830369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 121140382-T-C

http://identifiers.org/hco/12/GRCh38#64830440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121140311-C-A

64830440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121140311-C-T

http://identifiers.org/hco/12/GRCh38#64830491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121140260-C-A

64830514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140237-G-A

64830514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140237-G-T

64830525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140226-G-A

64830525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140226-G-T

http://identifiers.org/hco/12/GRCh38#64830531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121140220-C-A

64830562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140188-T-G

64830572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140178-A-G

http://identifiers.org/hco/12/GRCh38#64830595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121140156-C-A

64830634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140117-T-G

http://identifiers.org/hco/12/GRCh38#64830636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121140115-C-A

64830641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140110-G-A

64830641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140110-G-C

64830641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140110-G-T

64830703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140049-A-T

64830717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121140039-A-G

64831297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121139456-A-G

64831648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138727-A-G

64831770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138588-A-G

64831873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138481-C-T

64831889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138467-T-C

http://identifiers.org/hco/12/GRCh38#64832005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121138299-A-C

64832005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138299-A-T

64832024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138240-G-C

64832038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138184-T-G

64832058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138132-G-A

64832058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138132-G-T

64832099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138046-A-G

64832099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138046-A-T

64832105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121138040-T-C

64832161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121137983-G-A

64832331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137813-A-G

64832333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137811-G-T

64832353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137802-G-A

http://identifiers.org/hco/12/GRCh38#64832409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121137765-C-A

64832409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137765-C-T

64832420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137755-T-A

64832430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137745-T-C

64832438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137737-T-C

64832802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137411-C-T

http://identifiers.org/hco/12/GRCh38#64832826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121137393-C-A

64832839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137382-A-G

64832857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137364-G-A

64832889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137332-C-T

64832921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137325-A-G

64833043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121137223-G-C

64833230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121136787-A-G

64833342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121136695-G-A

64833652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135976-A-T

64833655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135973-G-A

64833676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135951-C-T

64833694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135945-T-C

http://identifiers.org/hco/12/GRCh38#64833702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121135937-A-C

64833702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135937-A-G

64833905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135668-G-T

64834108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121135127-C-T

64834330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121134909-A-T

64835139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121133833-A-G

64835148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121133824-T-C

64835463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121133561-A-G

64835862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121133377-T-C

64836239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121133033-T-C

http://identifiers.org/hco/12/GRCh38#64836343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121132927-A-C

64836472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121132785-T-A

http://identifiers.org/hco/12/GRCh38#64836725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121132524-C-A

64836725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121132524-C-T

64836920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121132315-G-A

64836948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121132292-T-C

http://identifiers.org/hco/12/GRCh38#64836973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121132272-A-C

64837590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121131721-A-T

64837852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121131585-C-T

64838064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121131411-G-A

64838087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121131389-T-A

http://identifiers.org/hco/12/GRCh38#64838396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121130944-A-C

64838452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130888-G-A

64838466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130874-A-G

64838534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130799-A-G

64838534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130799-A-T

64838591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130744-A-G

64838623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130718-A-G

64838661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130682-G-C

64838661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130682-G-T

64838985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130403-A-G

64838992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130396-G-A

64838992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121130396-G-T

64839566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121128622-G-T

64839605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121128584-A-G

64840097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121128058-A-G

http://identifiers.org/hco/12/GRCh38#64840173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121127988-C-A

64840173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121127988-C-G

64840872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126941-A-T

64841089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126725-A-G

64841205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126612-A-G

64841212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126603-G-A

64841380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126464-T-C

64841405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126425-C-T

64841595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126217-C-G

http://identifiers.org/hco/12/GRCh38#64841616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121126196-C-A

64841616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126196-C-T

64841642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121126170-T-C

64842733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121125366-T-G

64842925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121125180-T-G

64842962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121125157-A-G

64843159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121125052-C-T

64843324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124948-G-C

64843337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124935-G-T

64843338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124934-A-G

64843396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121124872-G-C

64843402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121124866-G-T

64843516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124754-G-A

http://identifiers.org/hco/12/GRCh38#64843525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121124745-C-A

64843525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124745-C-T

64843526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124744-G-A

64843526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124744-G-T

http://identifiers.org/hco/12/GRCh38#64843531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121124739-C-A

64843531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124739-C-T

64843574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124705-G-A

http://identifiers.org/hco/12/GRCh38#64843584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121124695-C-A

64843646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124338-C-T

64843735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124280-C-G

64843747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121124267-A-G

http://identifiers.org/hco/12/GRCh38#64859352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121121331-A-C

64859435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121121249-G-C

http://identifiers.org/hco/12/GRCh38#64859496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121121197-A-C

64859642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121121153-G-A

64859747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121121053-C-T

64859826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120976-C-T

64859832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120970-T-A

64860595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120638-G-A

http://identifiers.org/hco/12/GRCh38#64860660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121120572-C-A

64860905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120331-G-A

64860924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120313-T-C

64860948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120293-A-G

64860958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120283-G-A

64861169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121120105-G-T

64861439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121119806-G-A

64861671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121119307-T-A

64861700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121119274-T-G

64861900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121119053-G-T

64862030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118912-G-A

64862216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118731-A-G

64862282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118673-C-G

64862282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118673-C-T

64862398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118558-A-G

64862435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118505-A-G

64862470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118487-G-A

64862488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118470-G-A

64862592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121118384-A-G

64862830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121117707-G-A

64863151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121117429-A-G

http://identifiers.org/hco/12/GRCh38#64863169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121117411-C-A

http://identifiers.org/hco/12/GRCh38#64863177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121117373-C-A

64863177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121117373-C-G

http://identifiers.org/hco/12/GRCh38#64863572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121116837-C-A

64863715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121116686-G-A

64863970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121116212-G-A

http://identifiers.org/hco/12/GRCh38#64863976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121116209-A-C

http://identifiers.org/hco/12/GRCh38#64864108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121115975-C-A

64864108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121115975-C-T

64864170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121115862-T-C

64864211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121115821-A-G

64864629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121115152-T-C

64864640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121115141-A-T

64864668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 121115113-A-G

64864668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 121115113-A-T

64864686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121115095-C-T

64864818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121114761-G-A

64864839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121114738-T-A

64865011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121114563-C-T

64865022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121114552-A-G

64865030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121114545-C-T

64866671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121111859-T-C

http://identifiers.org/hco/12/GRCh38#64866686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121111844-A-C

http://identifiers.org/hco/12/GRCh38#64866689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121111841-C-A

64866770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121111764-T-C

64866819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121111715-G-A

64866819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121111715-G-C

64866831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121111703-G-A

64870380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121108288-A-G

64870473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121108211-G-A

64870473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121108211-G-T

http://identifiers.org/hco/12/GRCh38#64870499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121108189-C-A

64870563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121108134-C-T

http://identifiers.org/hco/12/GRCh38#64870764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121107942-A-C

64870809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 121107897-G-T

64870820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107886-C-G

64870822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107884-T-G

http://identifiers.org/hco/12/GRCh38#64870915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121107438-C-A

64870915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107438-C-T

http://identifiers.org/hco/12/GRCh38#64870916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121107437-C-A

64870916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107437-C-T

64870917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107436-A-G

http://identifiers.org/hco/12/GRCh38#64870922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121107429-C-A

64870922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107429-C-T

64870930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107420-G-A

64870930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107420-G-T

64870952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107398-G-C

64870952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107398-G-T

http://identifiers.org/hco/12/GRCh38#64870956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121107394-C-A

64871019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121107331-C-T

64871085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107265-C-T

64871358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106812-A-G

64871397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106768-T-C

64871404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106761-T-G

64871558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106597-A-T

64871619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106530-G-C

64871935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106277-C-T

http://identifiers.org/hco/12/GRCh38#64871938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121106274-C-A

64871938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106274-C-T

64872402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106115-G-T

64872408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106109-A-G

64872501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106031-T-C

64873274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105602-G-A

64873327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105561-G-C

64873331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105557-G-A

64873553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105327-A-G

64873725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105131-G-A

64873770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105083-A-G

64873986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104876-G-A

64874026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104837-T-C

64874052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104811-T-C

64874054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104807-A-G

64874115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104737-G-A

64874152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104701-A-T

64874820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103693-C-T

64874881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103627-G-A

64874882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103626-G-A

64874885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103623-A-G

64874936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103590-T-C

http://identifiers.org/hco/12/GRCh38#64874937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121103589-C-A

64874947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103581-A-G

64874949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103579-G-A

64874965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103563-G-C

64874965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121103563-G-T

http://identifiers.org/hco/12/GRCh38#64875009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121103519-C-A

http://identifiers.org/hco/12/GRCh38#64875079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121103449-A-C

64875181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103347-A-T

http://identifiers.org/hco/12/GRCh38#64875231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121103297-C-A

64875231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103297-C-G

64875264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103264-A-G

64875316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103212-G-T

64875318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103210-G-A

64875318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103210-G-T

64875357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103171-G-C

http://identifiers.org/hco/12/GRCh38#64875371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121103157-C-A

64875382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103134-G-A

64875444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103072-G-A

64875501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103015-G-T

http://identifiers.org/hco/12/GRCh38#64875510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121103006-A-C

64875510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103006-A-G

64875510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121103006-A-T

64875608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121102908-C-T

http://identifiers.org/hco/12/GRCh38#64875912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121102621-C-A

64875912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102621-C-G

64875912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102621-C-T

http://identifiers.org/hco/12/GRCh38#64875914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121102619-C-A

64875914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102619-C-G

64875914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102619-C-T

64875930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102603-T-A

64876034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102508-G-T

64876096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102446-T-A

64876096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102446-T-G

64876098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102444-G-A

64876098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102444-G-T

http://identifiers.org/hco/12/GRCh38#64876254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121102291-C-A

64876436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102045-A-G

http://identifiers.org/hco/12/GRCh38#64876438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121102043-C-A

64876438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102043-C-T

64876477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102005-G-A

64876477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121102005-G-T

64876504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101978-A-G

64876539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101947-T-C

http://identifiers.org/hco/12/GRCh38#64876549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121101937-C-A

64876585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101929-G-A

64876585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101929-G-T

64876639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101879-T-A

64876639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101879-T-C

http://identifiers.org/hco/12/GRCh38#64876932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121101603-C-A

64877009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101550-T-C

64877010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101549-A-G

http://identifiers.org/hco/12/GRCh38#64877011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121101546-C-A

64877083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101474-A-T

http://identifiers.org/hco/12/GRCh38#64877089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121101468-C-A

64877113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101444-C-T

64877116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101441-T-C

http://identifiers.org/hco/12/GRCh38#64877225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121101331-A-C

64877225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101331-A-G

http://identifiers.org/hco/12/GRCh38#64877324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121101242-C-A

64877431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121101135-G-T

64877740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100872-T-C

64877840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100756-G-T

64877955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100664-G-A

64878059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100609-G-A

64878059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100609-G-T

http://identifiers.org/hco/12/GRCh38#64878067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121100601-A-C

64878067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100601-A-G

http://identifiers.org/hco/12/GRCh38#64878240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121100433-A-C

64878259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100414-T-C

http://identifiers.org/hco/12/GRCh38#64878334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121100328-C-A

64878636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100049-G-C

64878667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121100018-C-T

64878741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099953-A-G

64878749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099945-A-G

http://identifiers.org/hco/12/GRCh38#64878755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121099932-C-A

64878755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099932-C-T

http://identifiers.org/hco/12/GRCh38#64878757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121099930-C-A

64878758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099929-A-G

64878758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099929-A-T

64878763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099923-G-A

64878801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099885-G-T

64878895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099767-A-G

64878970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29164
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121099692-A-G