http://identifiers.org/hco/11/GRCh38#73400773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100490869-C-A

73400773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100490869-C-T

73400828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100490811-T-C

73401507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100490149-G-T

http://identifiers.org/hco/11/GRCh38#73401760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100489899-C-A

73401804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489855-T-C

http://identifiers.org/hco/11/GRCh38#73401913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100489748-C-A

73401962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489685-A-G

73401962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489685-A-T

73401992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489655-T-A

73401994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489653-G-A

73402018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489627-G-T

http://identifiers.org/hco/11/GRCh38#73402050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100489593-C-A

73402050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489593-C-T

73402123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489521-T-C

http://identifiers.org/hco/11/GRCh38#73402330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100489353-A-C

73402381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489310-T-C

73402557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489131-G-T

73402648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100489020-T-C

73403115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488531-A-G

http://identifiers.org/hco/11/GRCh38#73403189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100488458-A-C

73403195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488452-G-T

http://identifiers.org/hco/11/GRCh38#73403286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100488348-C-A

73403345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488299-A-G

http://identifiers.org/hco/11/GRCh38#73403363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100488281-A-C

73403385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488272-T-C

73403408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488247-T-A

http://identifiers.org/hco/11/GRCh38#73403431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100488223-C-A

73403431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488223-C-T

73403458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488201-G-T

73403471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488188-G-A

73403471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100488188-G-T

73403753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100487951-G-A

73403753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100487951-G-T

73404158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 100487606-G-T

http://identifiers.org/hco/11/GRCh38#73404248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100487534-C-A

73404248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 100487534-C-T

73404342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100487436-G-A

73404342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100487436-G-T

http://identifiers.org/hco/11/GRCh38#73404417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100487359-C-A

73404458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100487323-T-C

http://identifiers.org/hco/11/GRCh38#73404731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100487077-C-A

73404889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100486928-G-T

73405135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100486742-T-C

73405278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100486616-G-A

73405278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3 prime UTR variant
orthologous variants: 100486616-G-T

http://identifiers.org/hco/11/GRCh38#73405765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100486143-C-A

73405765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100486143-C-T

73405828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100486079-G-T

73406076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100485864-T-A

73406076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100485864-T-C

73406166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100485778-G-C

http://identifiers.org/hco/11/GRCh38#73406467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100485505-C-A

73406485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100485481-G-A

73406485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100485481-G-T

73407358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100484808-A-G

73407408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100484767-G-A

73407408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100484767-G-T

http://identifiers.org/hco/11/GRCh38#73407462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100484722-C-A

http://identifiers.org/hco/11/GRCh38#73407745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100484432-A-C

http://identifiers.org/hco/11/GRCh38#73407768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100484410-C-A

73408364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100484207-T-C

73408490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100484138-G-A

73408619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100484076-A-G

73409183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100483683-G-T

73409235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100483634-G-A

http://identifiers.org/hco/11/GRCh38#73409355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100483524-C-A

73409357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100483522-T-C

http://identifiers.org/hco/11/GRCh38#73409368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100483506-A-C

73409642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100483233-G-A

73409690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100483166-G-A

73409690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100483166-G-T

73410092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100482758-A-T

http://identifiers.org/hco/11/GRCh38#73410732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100481321-A-C

http://identifiers.org/hco/11/GRCh38#73410825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100481225-C-A

73410849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100481201-C-T

73411023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100481007-C-T

73411313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100480743-T-C

73411527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, missense_variant
orthologous variants: 100480542-G-A

73411857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100480212-G-A

73411857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100480212-G-T

73411995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100479986-C-G

73412025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100479956-C-G

73412030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron variant
orthologous variants: 100479951-T-C

73412281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100479689-A-G

73412417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100479567-A-G

73414885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100477897-T-C

73414908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100477880-A-G

73415124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100477663-C-T

73415345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100477449-G-A

73417146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475960-G-A

73417146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475960-G-C

73417346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475748-A-G

73417425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475671-G-A

73417477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475639-A-T

73417792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475477-C-T

73417851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100475418-G-A

http://identifiers.org/hco/11/GRCh38#73419201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100474096-C-A

73419610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100473725-G-C

http://identifiers.org/hco/11/GRCh38#73419832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100473507-C-A

73419832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100473507-C-T

http://identifiers.org/hco/11/GRCh38#73419833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100473506-C-A

http://identifiers.org/hco/11/GRCh38#73420123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100473214-A-C

73420124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100473213-T-A

73420124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100473213-T-C

73420124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100473213-T-G

73420492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100472859-A-G

http://identifiers.org/hco/11/GRCh38#73420581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100472778-C-A

73420689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100472678-G-A

73420759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100472609-G-T

73420760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100472608-T-C

73421131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100472015-T-A

73421309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100471836-T-G

73421380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100471766-G-A

73421380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100471766-G-C

http://identifiers.org/hco/11/GRCh38#73421773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100471387-C-A

73421879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100471277-T-A

73422193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100470999-T-C

73422268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100470927-C-G

73422503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100470714-C-T

73422594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100470623-G-A

73423237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100470049-A-G

73423325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100469925-T-C

73423992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100468978-T-C

73424032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100468948-A-G

http://identifiers.org/hco/11/GRCh38#73424502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100468492-C-A

73424502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100468492-C-G

73424502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100468492-C-T

73425136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100467855-G-A

73425136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100467855-G-T

73426299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100467054-A-G

73426363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100466983-T-C

http://identifiers.org/hco/11/GRCh38#73426516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100466835-A-C

73426705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100466689-G-C

73426779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100466640-T-A

73427052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100466539-C-T

73427714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100465966-C-T

73427842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100465887-A-G

http://identifiers.org/hco/11/GRCh38#73428268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100465517-C-A

73428268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100465517-C-T

73428433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100465355-G-A

73428893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100464934-C-G

73429413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100463968-A-G

73429520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100463864-A-G

73429630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100463757-G-T

73429673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100463634-T-C

73429800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100463216-C-T

73429870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100463144-T-C

http://identifiers.org/hco/11/GRCh38#73430153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100462671-C-A

73430164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462658-G-T

73430170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462652-G-T

73430217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462605-C-G

73430217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462605-C-T

http://identifiers.org/hco/11/GRCh38#73430451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100462427-C-A

73430451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462427-C-T

http://identifiers.org/hco/11/GRCh38#73430555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100462333-C-A

73430646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462246-C-G

73430646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100462246-C-T

http://identifiers.org/hco/11/GRCh38#73430701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100462194-C-A

73430701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100462194-C-T

73430789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100462106-A-G

73434740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100457743-C-T

73434813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100457812-G-C

73434994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100457986-C-T

73435030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100458022-C-T

73435072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100458060-C-T

73435074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100458062-A-G

http://identifiers.org/hco/11/GRCh38#73435432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100458409-A-C

73438037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100456158-T-G

73438268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100455610-T-C

73438347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100455552-T-G

73438838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100455071-C-T

73438932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100454976-G-C

73439283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100454430-G-A

73439298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100454416-G-C

73439371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100454344-C-G

73439511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100454201-A-G

73439763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100453955-G-C

73440238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100453784-T-C

73440977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100453166-G-A

73440987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100453156-G-A

73441266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100452791-C-T

73441267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100452790-C-T

http://identifiers.org/hco/11/GRCh38#73457879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100449154-C-A

73458037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448982-A-G

73458048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100448976-T-C

73463886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446889-A-G

73463899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446875-A-T

73463913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446862-A-G

73463927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446851-C-T

73463984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100446803-A-G

73465317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442691-G-A

http://identifiers.org/hco/11/GRCh38#73465401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100442617-A-C

73465401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442617-A-G

73465506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442514-G-A

73465564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442445-T-A

73465564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442445-T-G

http://identifiers.org/hco/11/GRCh38#73465607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100442365-A-C

73465860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442123-A-G

73465966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100442059-A-G

73466040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441996-A-G

73466150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100441914-A-T

http://identifiers.org/hco/11/GRCh38#73466987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100438239-A-C

http://identifiers.org/hco/11/GRCh38#73466992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100438234-A-C

73467081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438168-G-A

73467126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100438115-T-A

73467314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100437981-T-C

73467750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100437657-T-C

73467969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100437461-C-T

73468613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435879-G-A

73468613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435879-G-C

73468613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435879-G-T

73468891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435644-A-G

73468903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435632-T-G

73468920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435615-T-C

http://identifiers.org/hco/11/GRCh38#73469011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100435522-C-A

73469011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100435522-C-T

73470237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100434505-A-G

http://identifiers.org/hco/11/GRCh38#73470288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100434459-A-C

73470380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100434377-G-A

73470609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100434177-C-T

73470657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100434128-G-A

73470912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100433878-T-C

73471015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100433799-C-T

http://identifiers.org/hco/11/GRCh38#73471192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100433495-C-A

73471278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100433420-G-A

73471311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100433391-T-C

73485775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100426513-C-T

73485943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100426355-C-T

73486811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100425527-T-C

73486865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100425502-T-G

73505871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100422513-G-A

73505890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100422490-T-A

73505972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100422411-A-G

73506085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100422306-C-T

http://identifiers.org/hco/11/GRCh38#73506217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100422183-C-A

73506217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100422183-C-T

73506456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100421342-T-C

73506456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100421342-T-G

73509268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100419190-T-C

73511552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100418359-G-A

73511720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100418250-A-G

73520457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100416426-T-C

73537865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100413727-C-T

73538367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412700-T-A

73538367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412700-T-C

73538367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412700-T-G

73538368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412699-G-A

73538416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412651-C-T

73538455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412612-T-C

http://identifiers.org/hco/11/GRCh38#73538463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100412604-C-A

73538559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100412509-T-C

73538938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100411155-T-C

http://identifiers.org/hco/11/GRCh38#73538985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100411107-C-A

73538985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100411107-C-T

73540044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100407968-C-T

73540157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100407852-A-T

73542577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404479-G-A

http://identifiers.org/hco/11/GRCh38#73542721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100404339-A-C

73542751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404127-T-C

73542943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100403777-C-T

73543000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100403727-T-C

73543002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100403725-T-C

http://identifiers.org/hco/11/GRCh38#73543692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100402733-C-A

73543692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100402733-C-T

73543744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100402682-C-G

73543826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100402600-G-A

73549710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100394874-C-T

73551140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100394494-T-A

73551140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100394494-T-C

73551140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100394494-T-G

73551417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100394215-G-A

73552083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100393552-C-T

73552100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100393535-G-T

73552124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100393508-T-C

73553215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389394-C-T

73553330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389276-T-C

73554131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388508-T-C

73554184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388434-G-A

73554184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388434-G-T

73565880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383695-A-G

73565946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383630-T-A

73565946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383630-T-C

73566223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383356-T-A

73566315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383267-G-A

73566420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383130-A-G

73566436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383110-A-G

http://identifiers.org/hco/11/GRCh38#73566607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100382885-C-A

73566644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382847-A-G

73566989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382580-A-G

73567025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382546-A-G

73567113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382474-G-A

73567242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100382353-T-C

http://identifiers.org/hco/11/GRCh38#73567255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100382347-A-C

73567675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381973-T-C

73567720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381873-A-G

73567783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381818-C-T

73567812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381786-G-C

73567944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381670-T-C

73567951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381663-C-T

73568141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381237-A-G

73568185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381175-T-C

http://identifiers.org/hco/11/GRCh38#73568970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100379972-C-A

73568970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379972-C-T

73568985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379958-G-C

73569203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379219-A-T

73569989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100378293-G-C

73570153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100377270-T-C

73570268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100377147-G-T

73570774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100376814-T-G

http://identifiers.org/hco/11/GRCh38#73570806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100376783-A-C

73570954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100376656-G-A

73571023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100376585-T-C

73573001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100376320-C-G

73573657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100375774-G-A

73574363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100375449-C-T

http://identifiers.org/hco/11/GRCh38#73574705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100375021-C-A

73574743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374969-T-A

73574746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374962-T-A

73574747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374961-A-G

73574747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374961-A-T

73574755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374953-G-A

73574755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374953-G-T

73574841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374849-G-C

73574846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374844-G-A

73575000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100374748-C-T

73575468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100373776-A-G

73575979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100373528-A-G

http://identifiers.org/hco/11/GRCh38#73576746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100372790-A-C

73577119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100372514-C-T

73577880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100371313-G-A

73577893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100371300-G-A

73577893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100371300-G-T

73577937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100371256-C-T

73578147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100371069-T-C

73578319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100370923-G-C

73578361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100370880-C-G

73578398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100370841-G-A

73578419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100370824-C-T

73578575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100370648-G-A

73579081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100369849-A-G

73579165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100369763-T-C

73579207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100369717-T-C

73579572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100369429-G-A

73590939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100365844-T-C

73591346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100364911-G-T

73593196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100360784-A-G

73593308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100360655-T-C

73593346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100360608-A-G

73593440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100360498-A-G

73593636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100360294-T-C

73593646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100360284-C-T

73593893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100359841-G-A

73594962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100359428-C-G

73595038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100359382-G-C

73595409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100358427-T-C

73595474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100358362-G-A

73595588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100358252-A-G

73596774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100357184-T-G

73597006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100357035-G-A

http://identifiers.org/hco/11/GRCh38#73597750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100356273-A-C

73597750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100356273-A-G

73597836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100356187-G-A

73597886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100356137-G-T

http://identifiers.org/hco/11/GRCh38#73597958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100356063-C-A

73597958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100356063-C-G

73597958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28999
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100356063-C-T