46979685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110483192-C-T

http://identifiers.org/hco/3/GRCh38#46979979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110482908-C-A

46979979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110482908-C-T

46980003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110482885-G-A

46981526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110481941-G-C

46982005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110481615-G-T

46982153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110481460-G-C

46982153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110481460-G-T

http://identifiers.org/hco/3/GRCh38#46982289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110481214-A-C

46982289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110481214-A-G

46982903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110480280-G-A

http://identifiers.org/hco/3/GRCh38#46983022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110480186-C-A

46983022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110480186-C-T

46983024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110480184-A-G

46983039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110480169-A-G

46983455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110479536-G-A

46983523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110479366-T-G

46983739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110479150-G-A

46983741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110479148-T-C

46984575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478760-T-C

46984645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478703-A-G

46984850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478482-G-A

46984990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478240-T-C

46985014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478216-T-C

46985047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478179-T-C

46985231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110478014-C-T

46985334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110477866-G-A

46985423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110477806-C-T

http://identifiers.org/hco/3/GRCh38#46985444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110477785-A-C

46985770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110477503-C-T

46986709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110476505-G-A

46987284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: 110474986-G-A

46987973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474439-G-T

46988102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474291-T-G

46988110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474284-G-A

46988110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474284-G-T

46988114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474280-G-T

http://identifiers.org/hco/3/GRCh38#46988162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110474231-A-C

46988162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474231-A-G

46988162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474231-A-T

http://identifiers.org/hco/3/GRCh38#46988167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110474226-A-C

46988167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474226-A-G

46988167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110474226-A-T

46988453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110473970-T-C

46988575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473866-A-G

46988575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473866-A-T

http://identifiers.org/hco/3/GRCh38#46988629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110473824-C-A

46988787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473666-A-T

46988821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473629-G-A

46988821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473629-G-C

46988856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 110473597-G-A

46988991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473457-A-G

46989251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473201-C-T

http://identifiers.org/hco/3/GRCh38#46989408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110473047-C-A

http://identifiers.org/hco/3/GRCh38#46989409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110473046-C-A

46989409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110473046-C-T

http://identifiers.org/hco/3/GRCh38#46989558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472813-C-A

46989558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 110472813-C-T

http://identifiers.org/hco/3/GRCh38#46989602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472769-C-A

46989602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110472769-C-T

http://identifiers.org/hco/3/GRCh38#46989627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472735-C-A

46989627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110472735-C-T

http://identifiers.org/hco/3/GRCh38#46989668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472707-C-A

46989668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110472707-C-G

http://identifiers.org/hco/3/GRCh38#46989723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472671-C-A

46989723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472671-C-G

46989723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472671-C-T

46989822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472556-T-G

46989938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472469-C-G

46989938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472469-C-T

46990171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472250-G-T

http://identifiers.org/hco/3/GRCh38#46990178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472244-C-A

http://identifiers.org/hco/3/GRCh38#46990201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472221-A-C

46990319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472128-A-G

46990557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110472031-A-G

http://identifiers.org/hco/3/GRCh38#46990601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110472014-A-C

46990818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110471860-G-A

46990938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110471735-G-A

46991428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant
orthologous variants: 110471337-G-A

46991494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant
orthologous variants: 110471271-C-T

46991550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant
orthologous variants: 110471215-G-A

46991550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant
orthologous variants: 110471215-G-T

46991699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110471066-G-A

46991699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110471066-G-C

http://identifiers.org/hco/3/GRCh38#46991924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110470859-C-A

46991924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 110470859-C-G

46991924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 110470859-C-T

http://identifiers.org/hco/3/GRCh38#46992356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110470647-C-A

46992356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110470647-C-T

http://identifiers.org/hco/3/GRCh38#46992419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110470591-A-C

46992419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110470591-A-G

46992482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant
orthologous variants: 110470550-T-A

46992653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110470362-G-T

46993138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469870-C-T

46993193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469815-G-A

46993394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469628-G-A

46993410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469613-C-G

http://identifiers.org/hco/3/GRCh38#46993796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110469068-C-A

46993796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469068-C-T

46993837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469027-T-A

http://identifiers.org/hco/3/GRCh38#46993839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110469025-C-A

46993839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110469025-C-T

46993906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110468958-G-T

http://identifiers.org/hco/3/GRCh38#46993970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110468896-C-A

46993970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110468896-C-G

46994072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468797-G-T

http://identifiers.org/hco/3/GRCh38#46994161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110468719-C-A

46994196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468687-G-A

http://identifiers.org/hco/3/GRCh38#46994221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110468662-C-A

46994221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468662-C-T

46994315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468570-G-A

46994315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468570-G-T

46994363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468524-A-G

46994401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468505-T-A

46994439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468472-A-G

46994525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110468388-A-G

46994540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110468373-A-T

46994811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468157-G-A

http://identifiers.org/hco/3/GRCh38#46994994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110468011-C-A

46994994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468011-C-T

http://identifiers.org/hco/3/GRCh38#46995003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110468002-C-A

46995003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468002-C-G

46995003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110468002-C-T

http://identifiers.org/hco/3/GRCh38#46995073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467931-C-A

http://identifiers.org/hco/3/GRCh38#46995113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467891-C-A

46995113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467891-C-G

46995113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467891-C-T

http://identifiers.org/hco/3/GRCh38#46995281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467723-C-A

http://identifiers.org/hco/3/GRCh38#46995308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467696-C-A

46995308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467696-C-T

46995336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467668-G-A

46995336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467668-G-T

http://identifiers.org/hco/3/GRCh38#46995400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467604-C-A

46995400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110467604-C-G

46995400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110467604-C-T

46995512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467492-C-G

46995512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467492-C-T

46995582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467422-C-G

http://identifiers.org/hco/3/GRCh38#46995668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467336-A-C

46995684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110467320-A-T

http://identifiers.org/hco/3/GRCh38#46995817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110467187-C-A

46995817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110467187-C-T

46995868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110467136-G-A

46995876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110467126-G-A

46996331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110466691-C-T

46996448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: stop gained
orthologous variants: 110466574-C-T

46996458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110466564-G-A

46996559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110466463-C-G

46996559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: stop gained
orthologous variants: 110466463-C-T

46996575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110466447-G-T

http://identifiers.org/hco/3/GRCh38#46996580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110466442-C-A

46996580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110466442-C-T

http://identifiers.org/hco/3/GRCh38#46996617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110466390-C-A

46996617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110466390-C-T

http://identifiers.org/hco/3/GRCh38#46996658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110466327-C-A

46996733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110466242-C-T

http://identifiers.org/hco/3/GRCh38#46996774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110466200-A-C

46996803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110466171-C-T

46997038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110465965-G-A

46997038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110465965-G-T

http://identifiers.org/hco/3/GRCh38#46997159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110465878-C-A

46997159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465878-C-T

46997249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465811-C-T

46997388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110465673-G-A

46997485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465564-G-A

http://identifiers.org/hco/3/GRCh38#46997513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110465541-A-C

46997513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465541-A-G

46997513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465541-A-T

46997628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110465427-C-T

46997680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110465375-G-A

46997680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110465375-G-C

46997698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465357-G-A

46997698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465357-G-T

46997707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465348-G-A

46997707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465348-G-T

http://identifiers.org/hco/3/GRCh38#46997792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110465316-C-A

46997792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465316-C-G

46997793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465315-T-A

46997826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465295-G-A

46997879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465249-G-T

46997934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110465201-C-T

46998074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465079-G-A

46998074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465079-G-C

46998074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465079-G-T

46998126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110465027-G-A

46998126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465027-G-C

46998126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465027-G-T

46998130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465023-G-T

46998142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110465011-A-G

46998406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464816-G-T

46998566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: splice donor variant
orthologous variants: 110464679-G-T

46998584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: 110464661-G-A

46998647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: 110464599-G-T

http://identifiers.org/hco/3/GRCh38#46998662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#110464579-C-A

46998673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: 110464568-G-A

46998673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: 110464568-G-C

46998673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, undefined
orthologous variants: 110464568-G-T

http://identifiers.org/hco/3/GRCh38#46998710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#110464524-C-A

46998710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 110464524-C-T

http://identifiers.org/hco/3/GRCh38#46998863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#110464380-C-A

46998863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, undefined
orthologous variants: 110464380-C-G

46998863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, undefined
orthologous variants: 110464380-C-T

46998868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110464375-G-A

46998868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110464375-G-T

46998887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 110464356-G-A

46999004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110464225-C-T

46999090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 110464139-G-A

46999090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 110464139-G-T

http://identifiers.org/hco/3/GRCh38#46999133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110464096-C-A

46999133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464096-C-G

46999133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464096-C-T

46999158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464071-G-A

46999158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464071-G-T

46999228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464022-C-T

http://identifiers.org/hco/3/GRCh38#46999244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110464003-C-A

46999244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110464003-C-T

http://identifiers.org/hco/3/GRCh38#46999327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110463926-C-A

46999327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110463926-C-T

46999354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110463899-C-T

46999523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110463677-A-G

46999523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110463677-A-T

46999528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110463602-A-G

46999528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110463602-A-T

46999735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463419-G-A

46999735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463419-G-C

46999770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463384-G-A

46999785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463370-C-T

46999798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463357-G-A

46999798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463357-G-T

46999852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463301-T-C

46999893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110463259-T-G

46999918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110463234-T-C

46999918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110463234-T-G

47000072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110463080-C-G

47000072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110463080-C-T

47000185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110462967-G-A

47000207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110462945-A-G

47000299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110462853-T-A

47000362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110462790-C-T

47000390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110462762-A-G

47000510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110462648-A-G

http://identifiers.org/hco/3/GRCh38#47000831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110462372-C-A

47000831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110462372-C-G

47000831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110462372-C-T

http://identifiers.org/hco/3/GRCh38#47000842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110462361-C-A

http://identifiers.org/hco/3/GRCh38#47000875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110462328-C-A

47000875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110462328-C-G

47000875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110462328-C-T

47000961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110462262-G-A

47000961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110462262-G-T

47000991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110462231-G-A

47001055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110462167-A-G

http://identifiers.org/hco/3/GRCh38#47001450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110461789-C-A

47001450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110461789-C-T

http://identifiers.org/hco/3/GRCh38#47001477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110461763-C-A

47001477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110461763-C-G

47001477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110461763-C-T

47001480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110461760-G-A

47001480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110461760-G-T

47001749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110461433-G-A

http://identifiers.org/hco/3/GRCh38#47001915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110461273-C-A

47002043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110461145-T-C

47002102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: synonymous variant
orthologous variants: 110461110-A-T

47002337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110460871-A-G

47002452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110460754-T-A

47002452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110460754-T-C

http://identifiers.org/hco/3/GRCh38#47002678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110460532-C-A

47002678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 110460532-C-T

http://identifiers.org/hco/3/GRCh38#47002734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110460476-C-A

47002734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 110460476-C-T

47002910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110460242-G-T

47002918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110460235-A-G

47002997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110460151-A-G

47003151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110460008-T-G

http://identifiers.org/hco/3/GRCh38#47003164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459995-C-A

47003164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459995-C-T

47003186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110459973-T-A

47003287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense variant
orthologous variants: 110459872-G-A

47003343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459830-G-T

47003378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459804-T-C

47003518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459685-G-A

http://identifiers.org/hco/3/GRCh38#47003653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459556-C-A

47003653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459556-C-T

47003685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459530-G-C

47003685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459530-G-T

47003715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459502-A-G

http://identifiers.org/hco/3/GRCh38#47003728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459490-C-A

47003728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459490-C-T

http://identifiers.org/hco/3/GRCh38#47003733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459485-C-A

47003753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459476-C-T

47003774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459455-G-C

47003774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron variant
orthologous variants: 110459455-G-T

47003943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110459289-G-A

http://identifiers.org/hco/3/GRCh38#47003958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459274-C-A

47003958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110459274-C-T

47003999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110459233-A-G

http://identifiers.org/hco/3/GRCh38#47004024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459208-C-A

47004038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110459194-G-C

47004154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110459075-G-A

47004154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110459075-G-C

http://identifiers.org/hco/3/GRCh38#47004225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110459004-A-C

47004225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110459004-A-G

47004446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458778-A-T

47004709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458555-G-A

47004709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458555-G-T

47004723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458538-G-A

47004723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458538-G-T

http://identifiers.org/hco/3/GRCh38#47004866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110458416-C-A

47004866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458416-C-T

47004913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110458370-A-G

47005165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110458100-C-T

47005169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110458096-C-T

47005281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110457984-G-A

47005290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110457975-A-G

47005352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457923-G-A

47005352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457923-G-C

47005352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457923-G-T

http://identifiers.org/hco/3/GRCh38#47005410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110457883-C-A

47005410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457883-C-T

47005699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457606-G-A

http://identifiers.org/hco/3/GRCh38#47005804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110457503-C-A

47005833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110457474-C-T

47005838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110457469-C-T

47005896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457416-T-C

47005917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457398-T-A

47005918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457397-G-A

http://identifiers.org/hco/3/GRCh38#47005928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110457387-C-A

47006018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110457298-G-C

47006021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110457295-G-A

47006021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110457295-G-C

47006444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110456878-G-A

47006444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110456878-G-T

http://identifiers.org/hco/3/GRCh38#47006471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456851-A-C

http://identifiers.org/hco/3/GRCh38#47006499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456826-C-A

47006499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110456826-C-G

http://identifiers.org/hco/3/GRCh38#47006518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456808-C-A

47006518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110456808-C-T

47006792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110456669-G-T

47006816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110456647-G-C

http://identifiers.org/hco/3/GRCh38#47006957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456507-C-A

http://identifiers.org/hco/3/GRCh38#47007042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456448-C-A

47007042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110456448-C-T

http://identifiers.org/hco/3/GRCh38#47007114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456376-C-A

47007114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 110456376-C-T

47007141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110456349-T-C

47007148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110456342-A-G

47007192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110456301-T-A

http://identifiers.org/hco/3/GRCh38#47007398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456097-C-A

47007398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110456097-C-G

47007398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110456097-C-T

http://identifiers.org/hco/3/GRCh38#47007471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110456024-C-A

47007503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455992-G-A

47007503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455992-G-T

http://identifiers.org/hco/3/GRCh38#47007535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110455961-C-A

http://identifiers.org/hco/3/GRCh38#47007561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110455935-C-A

47007561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110455935-C-G

47007595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455901-C-T

47007652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455844-G-A

47007713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455783-G-T

47007719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455777-G-A

47007719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455777-G-C

47007780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455725-C-G

http://identifiers.org/hco/3/GRCh38#47007816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#110455696-A-C

47008036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110455451-G-C

47008070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 110455399-G-A

47008118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110455351-G-C

47008365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110455105-C-G

47008962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454558-T-G

http://identifiers.org/hco/3/GRCh38#47008996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110454523-C-A

47008996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110454523-C-T

47009026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110454493-G-A

47009026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110454493-G-T

http://identifiers.org/hco/3/GRCh38#47009095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#110454424-A-C

47009095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110454424-A-T

47009363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110454159-T-C

http://identifiers.org/hco/3/GRCh38#47009380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110454138-C-A

47009380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110454138-C-G

47009380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110454138-C-T

http://identifiers.org/hco/3/GRCh38#47009392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110454126-C-A

47009392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110454126-C-T

47009594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3 prime UTR variant
orthologous variants: 110453969-G-A

47009594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3 prime UTR variant
orthologous variants: 110453969-G-C

47009594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3 prime UTR variant
orthologous variants: 110453969-G-T

http://identifiers.org/hco/3/GRCh38#47009684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31928
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110453877-A-C