76357838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3 prime UTR variant
orthologous variants: 83023758-C-T

76357934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3 prime UTR variant
orthologous variants: 83023645-G-A

76358154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3 prime UTR variant
orthologous variants: 83023420-C-T

76358466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83023122-G-C

http://identifiers.org/hco/18/GRCh38#76358551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83023051-C-A

76358551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83023051-C-T

76358602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022998-A-G

76358638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022965-C-G

76358845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022851-A-G

76358845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022851-A-T

76358846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022850-A-G

http://identifiers.org/hco/18/GRCh38#76358966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83022785-C-A

76359036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022742-A-G

76359074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022721-T-C

76359124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022669-G-A

76359124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022669-G-C

76359143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022642-G-A

76359143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022642-G-C

76359143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022642-G-T

http://identifiers.org/hco/18/GRCh38#76359157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83022628-C-A

76359157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022628-C-T

76359214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83022588-T-C

http://identifiers.org/hco/18/GRCh38#76359249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83022551-C-A

76359320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022483-G-T

76359352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022451-G-A

76359384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022425-A-G

76359393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022416-G-C

76359401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022408-G-A

76359548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022270-G-A

76359548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022270-G-C

76359597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022209-G-A

76359597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022209-G-C

76359597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022209-G-T

76359600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022206-A-G

76359600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022206-A-T

76359755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022050-G-A

76359755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83022050-G-T

76359846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021982-A-G

76360013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021813-C-T

http://identifiers.org/hco/18/GRCh38#76360070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83021758-C-A

76360134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021728-G-A

76360134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021728-G-T

http://identifiers.org/hco/18/GRCh38#76360149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83021713-C-A

76360149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021713-C-T

http://identifiers.org/hco/18/GRCh38#76360186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83021679-C-A

76360186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021679-C-T

76360187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021678-A-G

76360187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021678-A-T

76360188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021677-C-G

76360188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021677-C-T

76360236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021638-G-A

76360260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021614-A-T

76360573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021335-A-T

76360640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021251-A-G

76360642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021249-A-T

76360644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021247-A-T

76360646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83021245-A-T

http://identifiers.org/hco/18/GRCh38#76360687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83021178-C-A

http://identifiers.org/hco/18/GRCh38#76360849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83021014-C-A

76360946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020934-C-T

76360948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020932-G-A

76360948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020932-G-T

76361167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020711-C-T

76361358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020522-A-G

76361382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020498-G-T

76361423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020457-G-T

76361425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020455-A-G

http://identifiers.org/hco/18/GRCh38#76361439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83020441-C-A

76361441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020439-T-C

76361460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020420-A-G

76361470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020410-G-T

76361625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020260-A-G

76361861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020028-A-G

76361862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83020027-T-C

76361933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019953-G-A

76361979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019901-G-A

http://identifiers.org/hco/18/GRCh38#76362017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83019872-C-A

http://identifiers.org/hco/18/GRCh38#76362058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83019837-C-A

76362208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019704-T-C

76362354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019593-G-A

76362354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019593-G-T

76362363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019583-G-A

76362363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019583-G-T

76362365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019581-G-A

76362365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019581-G-T

http://identifiers.org/hco/18/GRCh38#76362372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83019574-C-A

76362372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019574-C-T

76362405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019542-A-G

76362424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019523-G-A

76362434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019513-G-A

76362436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019511-G-A

76362436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83019511-G-C

76362544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83019409-G-A

76362581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83019374-A-G

http://identifiers.org/hco/18/GRCh38#76362658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83019306-C-A

76362658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83019306-C-G

76362658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83019306-C-T

76362862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83019167-G-T

76362915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83019110-G-C

76363063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018972-C-T

76363091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018944-G-A

76363209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018862-G-A

76363274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018800-A-G

76363891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018171-G-A

76363917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018151-C-T

76363943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018124-T-C

76364058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83018030-A-G

76364209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017897-G-A

76364251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017856-T-A

76364556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017619-G-A

76364703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017467-G-T

76364914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017177-A-G

76364929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017149-G-A

76364929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017149-G-C

76364942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017120-A-G

76365029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83017020-G-C

76365086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83016963-G-A

76365098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83016951-T-A

http://identifiers.org/hco/18/GRCh38#76365118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83016939-A-C

76365145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83016912-G-A

76368162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83014458-T-C

76368241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83014388-T-C

76368344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83014299-T-C

http://identifiers.org/hco/18/GRCh38#76368527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83014125-C-A

76368527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83014125-C-T

76368578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83014085-C-T

76368707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83013970-T-C

76368914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83013803-A-G

76368977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83013748-G-A

76370150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012988-T-G

76370483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012700-G-A

76370483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012700-G-C

76370483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012700-G-T

http://identifiers.org/hco/18/GRCh38#76370620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83012568-C-A

76370620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012568-C-T

76370626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012562-A-G

76370627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012561-G-A

76370627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012561-G-C

76370627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012561-G-T

http://identifiers.org/hco/18/GRCh38#76370662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83012529-C-A

76370675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012516-A-G

76370675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012516-A-T

http://identifiers.org/hco/18/GRCh38#76370699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83012495-A-C

76370699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012495-A-T

http://identifiers.org/hco/18/GRCh38#76370733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83012461-C-A

76370733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012461-C-T

http://identifiers.org/hco/18/GRCh38#76371003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83012219-C-A

76371003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012219-C-T

76371004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012218-G-A

76371020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012198-C-T

76371038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012182-T-G

76371057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83012164-G-A

http://identifiers.org/hco/18/GRCh38#76371118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83012114-A-C

76371501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83011278-G-A

76371501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83011278-G-T

76371665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83011132-A-T

76371697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83011100-G-T

76371731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83011071-T-C

76371793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83011011-C-G

76371793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83011011-C-T

76371890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83010952-C-T

76371983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83010861-C-G

76372010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83010833-G-A

76373715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008826-G-A

76374077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008496-G-A

76374264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008343-T-C

76374344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008273-C-G

76374356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008264-T-C

76374468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008154-G-A

76374490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008138-T-A

76374490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008138-T-C

76374510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83008113-G-A

76378480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006587-T-C

76378515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006558-G-A

76378628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006477-G-A

76378694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006430-C-T

76378717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006407-T-A

76378741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006393-G-A

76378741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006393-G-T

http://identifiers.org/hco/18/GRCh38#76378841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83006335-C-A

76378904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83006272-C-G

76378904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83006272-C-T

http://identifiers.org/hco/18/GRCh38#76379095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#83006090-C-A

76379378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83005810-A-G

76379580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83005608-G-A

76379580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83005608-G-C

76379975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83005219-C-T

76380251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83004919-G-C

76381649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003062-G-C

76381649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003062-G-T

76381775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002968-C-T

76381778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002965-A-T

http://identifiers.org/hco/18/GRCh38#76418575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82989194-C-A

76418584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82989185-C-T

76418836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82988937-A-G

76418927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82988863-A-T

76427464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82985315-T-C

76427466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82985313-T-C

76427494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82985286-A-T

76427532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82985248-A-G

76427911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82984863-C-T

76427998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82984783-C-T

76428634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82983293-G-C

76428924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82983002-T-C

76428942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82982985-T-C

76430814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82981369-A-G

76431015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82981162-T-C

76431087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82980980-G-A

76431330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82980769-G-A

76431330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82980769-G-T

76438366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82979746-A-T

76438409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82979715-T-C

76438585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82979582-G-A

76439671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82978188-A-G

76440377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977417-C-T

76440402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977393-G-A

76440402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977393-G-T

76440573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977243-C-T

76440596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977220-T-A

76440596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977220-T-C

76440604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977209-T-C

76440725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977078-A-G

76440727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977076-T-C

76440727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977076-T-G

76440776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82977014-A-G

76440923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975830-T-C

76440954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975798-G-T

76440983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975775-A-G

76440983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975775-A-T

76441024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975751-G-A

76441024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975751-G-T

76441060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975705-G-T

76441117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975633-T-C

http://identifiers.org/hco/18/GRCh38#76441120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82975630-C-A

76441120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975630-C-G

76441120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82975630-C-T

76441258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82975559-A-G

http://identifiers.org/hco/18/GRCh38#76441430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82975393-C-A

76441430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82975393-C-G

76441430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82975393-C-T

http://identifiers.org/hco/18/GRCh38#76441745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82975078-C-A

76441745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82975078-C-T

http://identifiers.org/hco/18/GRCh38#76441856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82974967-C-A

76441856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974967-C-G

76441856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974967-C-T

76441889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974934-A-G

76442426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974394-A-G

http://identifiers.org/hco/18/GRCh38#76442507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82974313-A-C

76442528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974292-C-T

76442535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974285-C-T

76442564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974256-G-A

76442564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974256-G-T

http://identifiers.org/hco/18/GRCh38#76442612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82974208-C-A

76442612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974208-C-T

76442681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974175-T-C

76442744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82974112-T-A

http://identifiers.org/hco/18/GRCh38#76442770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82974086-C-A

76442770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82974086-C-G

76442770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82974086-C-T

76443059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973797-A-G

76443145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973706-A-G

76443145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973706-A-T

76443168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973683-G-A

76443168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973683-G-T

76443201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973657-G-A

76443201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82973657-G-T

http://identifiers.org/hco/18/GRCh38#76443243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82973612-C-A

76443243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82973612-C-T

76443264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82973589-G-A

76443264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82973589-G-C

76443264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82973589-G-T

http://identifiers.org/hco/18/GRCh38#76443320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82973533-A-C

76443320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82973533-A-G

76443369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82973499-T-C

76446798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82970461-C-G

76446834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82970428-G-C

76447285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82970068-C-T

76447404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82969955-A-G

76447595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82969803-T-C

76447640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82969743-T-C

76447803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82969631-T-C

76448109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82969410-T-G

http://identifiers.org/hco/18/GRCh38#76448138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82969382-A-C

76448143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82969377-T-C

76448693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82968944-G-A

76448754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82968871-G-A

76448945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82968644-T-C

76448988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82968602-T-C

76449757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967658-C-T

76449814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967601-G-C

76449963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967461-T-C

76449963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967461-T-G

76450012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967415-A-G

76450051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967376-C-G

76450051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967376-C-T

76450154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967328-T-C

http://identifiers.org/hco/18/GRCh38#76450183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82967307-A-C

76450185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967303-G-A

http://identifiers.org/hco/18/GRCh38#76450204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82967283-C-A

76450204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967283-C-G

76450204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967283-C-T

76450322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82967167-T-G

76450568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966985-G-C

76450583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966970-G-A

76450583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966970-G-T

76450862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966790-T-C

76451013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966637-C-T

76451014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966636-G-A

http://identifiers.org/hco/18/GRCh38#76451018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82966632-A-C

76451018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966632-A-G

http://identifiers.org/hco/18/GRCh38#76451019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82966631-A-C

76451049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966574-G-T

76451058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966533-G-C

76451168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966341-C-G

76451168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966341-C-T

76451257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966256-G-A

http://identifiers.org/hco/18/GRCh38#76451305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82966203-C-A

76451305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966203-C-T

76451358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82966153-G-C

76451840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82965709-T-C

76452090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82965491-G-A

76452159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82965440-C-G

76452485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82965154-T-C

76452508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82965131-G-C

76452563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82965116-C-T

76452857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964945-G-C

76452897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964911-G-A

http://identifiers.org/hco/18/GRCh38#76453214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82964628-C-A

76453214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964628-C-T

76453291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964571-T-C

76453344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964520-C-T

76453375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964489-G-T

76453423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964441-A-G

76453481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964394-A-G

76453489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964386-A-T

76453599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964251-C-T

76453710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82964146-T-C

76454009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963937-C-T

76454050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963897-G-A

76454160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963800-G-A

76454160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963800-G-C

76454247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963720-C-T

76454331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963657-T-A

76454331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963657-T-C

76454714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963296-C-T

76454866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963148-C-T

76455008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82963031-C-T

http://identifiers.org/hco/18/GRCh38#76455158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82962917-A-C

http://identifiers.org/hco/18/GRCh38#76455255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82962787-A-C

http://identifiers.org/hco/18/GRCh38#76455364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82962666-C-A

76455474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82962551-T-C

76455562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82962479-G-C

76455584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82962461-C-G

76455590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82962456-A-G

76455620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82962428-C-T

76456845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961605-T-C

76456879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961572-G-A

76456934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961515-T-C

76456939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961510-T-C

76456971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961495-C-T

76457028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961441-T-A

http://identifiers.org/hco/18/GRCh38#76457169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82961323-A-C

76457169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961323-A-G

76457359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82961081-C-T

http://identifiers.org/hco/18/GRCh38#76461563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82958300-A-C

76468931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82954992-C-G

76468935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82954988-A-G

76469155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82954790-G-C

76469266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82954681-A-G

76469337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82954601-T-C

76469474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82954018-T-C

76469566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82953944-G-C

76469627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82953889-A-G

76469693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82953823-C-T

http://identifiers.org/hco/18/GRCh38#76469699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82953817-A-C

76469699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82953817-A-G

76475813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82947489-T-A

76475813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82947489-T-C

76476056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82947253-G-C

76477418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82945523-G-A

76477554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82945412-G-A

http://identifiers.org/hco/18/GRCh38#76482838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82941644-C-A

76482838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82941644-C-T

76484154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82939782-A-G

76484308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82939620-G-C

76484959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938909-C-T

76485142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938755-T-C

76485328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938565-A-G

76485461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938457-A-G

76485493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938425-G-C

76485517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938402-C-T

http://identifiers.org/hco/18/GRCh38#76485619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82938306-C-A

76485619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938306-C-T

76485689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938242-A-G

76485805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938129-C-T

76485827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938107-T-C

76485849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938082-G-C

76485849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938082-G-T

76485850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82938081-T-A

76486012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937904-A-G

76486042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937877-G-A

76486161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937778-C-T

76486281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937662-T-A

76486287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937656-C-T

76486425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937512-G-T

76486578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937346-C-G

76486749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937179-A-G

76486819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937131-G-A

76486842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82937105-A-G

76487127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82936851-T-C

76487229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82936748-C-G

76487610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82936378-A-G

http://identifiers.org/hco/18/GRCh38#76487868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#82936108-C-A

76487869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82936107-A-G

76487905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82936062-A-G

http://identifiers.org/hco/18/GRCh38#76488535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82935565-A-C

76488535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82935565-A-G

76488535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82935565-A-T

76488665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82935448-A-G

76489196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82934896-A-G

76489454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82934639-G-A

76489456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82934637-G-C

76489456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82934637-G-T

http://identifiers.org/hco/18/GRCh38#76489546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82934548-A-C

76489581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82934518-T-A

76489581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82934518-T-C

76489717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82934398-T-C

76490192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933918-C-T

76490283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933838-T-C

76490381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933746-T-C

76490463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933672-G-A

76490463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933672-G-C

76490608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933529-T-C

76490981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82933205-G-A

76490987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82933199-C-T

76491008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82933180-G-A

76491012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82933176-C-T

76491017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 82933171-G-A

76491065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 82933132-G-A

http://identifiers.org/hco/18/GRCh38#76491156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82933037-A-C

76491156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933037-A-G

76491190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933003-C-G

76491190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933003-C-T

76491191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933002-G-A

76491191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82933002-G-C

http://identifiers.org/hco/18/GRCh38#76491202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82932992-C-A

76491202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82932992-C-T

76491566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82932729-C-G

http://identifiers.org/hco/18/GRCh38#76491594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82932700-C-A

76491594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82932700-C-G

76491594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82932700-C-T

76491764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82932516-G-A

76491764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82932516-G-T

http://identifiers.org/hco/18/GRCh38#76491786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82932474-C-A

76492003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82932278-G-A

76492091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82932202-T-C

76492399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82931922-G-A

http://identifiers.org/hco/18/GRCh38#76492417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931904-C-A

76492464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82931872-A-G

http://identifiers.org/hco/18/GRCh38#76492471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931865-C-A

76492547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82931803-T-A

76492547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82931803-T-C

76492580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82931770-T-C

http://identifiers.org/hco/18/GRCh38#76492798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931576-C-A

76492851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931519-A-G

76492851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931519-A-T

76492908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931462-G-A

76492908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931462-G-T

http://identifiers.org/hco/18/GRCh38#76492919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931451-C-A

76492919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82931451-C-T

http://identifiers.org/hco/18/GRCh38#76492936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931434-C-A

76492936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931434-C-G

76492936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931434-C-T

http://identifiers.org/hco/18/GRCh38#76493041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931334-C-A

76493041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931334-C-T

http://identifiers.org/hco/18/GRCh38#76493058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931317-C-A

76493058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931317-C-G

76493189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931194-C-T

76493235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931150-T-C

http://identifiers.org/hco/18/GRCh38#76493307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82931088-A-C

76493307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931088-A-T

76493333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931074-G-A

76493333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931074-G-T

76493336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931071-G-T

76493363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931048-G-A

76493363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82931048-G-C

http://identifiers.org/hco/18/GRCh38#76493430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82930982-C-A

76493686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82930725-A-T

http://identifiers.org/hco/18/GRCh38#76494444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#82929827-A-C

76494444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, undefined
orthologous variants: 82929827-A-G

76494848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82929414-C-T

76495079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82929191-G-A

76495096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82929167-C-T

http://identifiers.org/hco/18/GRCh38#76495128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#82929131-C-A

76495128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82929131-C-G

76495128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron variant
orthologous variants: 82929131-C-T

76495654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82928601-C-T

76495685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82928556-T-C

76495710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82928531-T-C

76496040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28990
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82928245-C-T