http://identifiers.org/hco/10/GRCh38#93060807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37673705-C-A

93060807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5 prime UTR variant
orthologous variants: 37673705-C-T

93061000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37673876-G-T

93061083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37673953-T-A

93061083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37673953-T-C

93061083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37673953-T-G

93061112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37673978-T-A

93061112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37673978-T-C

93061112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37673978-T-G

http://identifiers.org/hco/10/GRCh38#93061133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37674002-C-A

93061177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37674045-G-A

93061177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37674045-G-T

93061256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37674120-G-C

93061256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37674120-G-T

93061315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37674179-G-A

93061315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37674179-G-T

93061323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674187-G-A

93061323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674187-G-C

93061323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674187-G-T

93061329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674193-G-A

93061329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674193-G-C

93061329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674193-G-T

93061600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674440-G-A

93061600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674440-G-T

http://identifiers.org/hco/10/GRCh38#93061601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37674441-C-A

93061601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674441-C-T

http://identifiers.org/hco/10/GRCh38#93061610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37674447-C-A

93061610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674447-C-T

93061611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674448-G-A

93061611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674448-G-T

http://identifiers.org/hco/10/GRCh38#93061860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37674716-A-C

93061860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674716-A-G

93061917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674777-G-T

93061945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37674822-G-A

93062045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 37674920-T-A

http://identifiers.org/hco/10/GRCh38#93062099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37674974-C-A

93062099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37674974-C-T

93062195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37675070-G-T

http://identifiers.org/hco/10/GRCh38#93062210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675085-C-A

93062210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37675085-C-G

93062210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37675085-C-T

http://identifiers.org/hco/10/GRCh38#93062346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675213-C-A

http://identifiers.org/hco/10/GRCh38#93062348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675215-C-A

93062348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675215-C-T

93062360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675228-G-A

93062360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675228-G-C

93062360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675228-G-T

93062362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675230-G-A

93062362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675230-G-T

93062368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675236-T-A

93062368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675236-T-C

http://identifiers.org/hco/10/GRCh38#93062384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675253-C-A

93062384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675253-C-T

http://identifiers.org/hco/10/GRCh38#93062431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675302-C-A

93062578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675440-G-A

93062578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675440-G-T

http://identifiers.org/hco/10/GRCh38#93062615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675467-C-A

93062615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37675467-C-T

http://identifiers.org/hco/10/GRCh38#93062696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675543-C-A

93062696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37675543-C-G

93062696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37675543-C-T

93062700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37675547-G-A

93062700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37675547-G-T

http://identifiers.org/hco/10/GRCh38#93062770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675617-C-A

93062770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37675617-C-T

93062780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37675627-G-A

93062780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37675627-G-T

93062914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37675761-C-G

93062914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37675761-C-T

93062935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37675782-G-A

93062935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37675782-G-T

93062972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37675819-G-A

93062972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37675819-G-T

93063116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37675909-G-A

93063116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37675909-G-T

http://identifiers.org/hco/10/GRCh38#93063222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37675998-C-A

93063222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37675998-C-G

93063233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676009-G-A

93063233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676009-G-T

http://identifiers.org/hco/10/GRCh38#93063321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676081-C-A

93063321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676081-C-T

http://identifiers.org/hco/10/GRCh38#93063325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676085-C-A

http://identifiers.org/hco/10/GRCh38#93063327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676087-C-A

93063336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676096-G-A

93063336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676096-G-T

http://identifiers.org/hco/10/GRCh38#93063340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676100-C-A

93063370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676129-G-A

93063370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676129-G-T

93063379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676136-G-T

93063391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676148-A-G

http://identifiers.org/hco/10/GRCh38#93063430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676177-C-A

93063430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676177-C-T

93063443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676190-G-A

93063473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676223-A-G

93063473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676223-A-T

93063509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676258-G-A

93063509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676258-G-T

93063540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676283-G-A

93063540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676283-G-T

http://identifiers.org/hco/10/GRCh38#93063591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676332-C-A

93063591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676332-C-T

93063682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676404-G-T

93063751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676468-T-A

93063859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676571-G-T

93063878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676590-G-A

93063878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676590-G-T

93063902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676614-C-T

93063948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676667-C-T

93063953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676672-G-A

93063968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676684-G-A

93063968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676684-G-T

93064032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676764-G-T

http://identifiers.org/hco/10/GRCh38#93064058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676783-C-A

93064058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676783-C-T

93064059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676784-A-G

93064071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676796-G-A

93064071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676796-G-T

http://identifiers.org/hco/10/GRCh38#93064077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676802-C-A

93064077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676802-C-G

93064077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676802-C-T

http://identifiers.org/hco/10/GRCh38#93064104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676827-C-A

93064104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676827-C-T

93064127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676849-C-T

93064191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676903-G-A

93064191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676903-G-T

http://identifiers.org/hco/10/GRCh38#93064225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37676937-C-A

93064225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676937-C-G

93064245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676961-G-A

93064245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37676961-G-C

http://identifiers.org/hco/10/GRCh38#93064334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677229-C-A

93064334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677229-C-G

93064334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677229-C-T

http://identifiers.org/hco/10/GRCh38#93064442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677339-A-C

93064447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37677344-G-A

93064447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37677344-G-T

http://identifiers.org/hco/10/GRCh38#93064553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677450-C-A

93064553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677450-C-G

93064553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677450-C-T

http://identifiers.org/hco/10/GRCh38#93064618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677561-C-A

93064618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37677561-C-T

http://identifiers.org/hco/10/GRCh38#93064645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677590-C-A

93064645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37677590-C-G

93064645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37677590-C-T

93064667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37677612-G-A

93064667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37677612-G-T

http://identifiers.org/hco/10/GRCh38#93064782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677704-C-A

http://identifiers.org/hco/10/GRCh38#93064822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677741-C-A

http://identifiers.org/hco/10/GRCh38#93064825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677744-C-A

93064825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677744-C-T

http://identifiers.org/hco/10/GRCh38#93064870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37677781-C-A

93064975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677880-T-G

93065018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677944-G-A

93065018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677944-G-T

93065037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677967-A-T

93065069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37677999-A-G

93065215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678116-G-A

93065562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678840-A-G

93065615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678891-T-C

93065693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678948-G-T

93065713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678965-C-T

93065738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678986-T-A

93065738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37678986-T-C

93065826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37679069-A-G

93065937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37679139-G-A

93065937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37679139-G-C

93065937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37679139-G-T

93066033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37679235-G-A

93066033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37679235-G-T

93066108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679310-G-A

93066108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679310-G-C

93066108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679310-G-T

http://identifiers.org/hco/10/GRCh38#93066138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37679328-C-A

93066138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37679328-C-G

http://identifiers.org/hco/10/GRCh38#93066143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37679333-C-A

93066143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37679333-C-T

http://identifiers.org/hco/10/GRCh38#93066261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37679451-C-A

93066261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679451-C-G

93066261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679451-C-T

93066267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679457-G-A

93066267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 37679457-G-T

http://identifiers.org/hco/10/GRCh38#93066366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37679517-C-A

93066366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37679517-C-G

93066366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37679517-C-T

http://identifiers.org/hco/10/GRCh38#93066621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37679783-C-A

93066675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37679814-C-T

93066857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680003-G-A

93066857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680003-G-C

93066937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680082-C-T

93067021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680162-G-T

93067178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680256-G-C

93067357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680364-A-T

93067370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680377-T-C

93067371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680378-C-G

93067708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37680776-G-A

93068147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37681212-A-T

93068200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37681260-A-T

93068288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37681349-G-T

93068298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37681359-T-G

93068421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37681479-G-A

http://identifiers.org/hco/10/GRCh38#93068484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37681542-C-A

93068484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37681542-C-T

93068535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37681593-C-G

93068535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37681593-C-T

93068547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37681605-T-C

93068599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37681657-G-A

93068599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37681657-G-T

http://identifiers.org/hco/10/GRCh38#93068702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37681760-C-A

93068783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681836-G-A

93068783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681836-G-C

93068783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681836-G-T

http://identifiers.org/hco/10/GRCh38#93068784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37681837-C-A

93068863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681902-A-G

93068864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681903-G-T

93068904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681942-G-T

http://identifiers.org/hco/10/GRCh38#93068905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37681943-C-A

93068905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681943-C-G

93068905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37681943-C-T

http://identifiers.org/hco/10/GRCh38#93068950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37681986-A-C

http://identifiers.org/hco/10/GRCh38#93069009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37682048-C-A

93069009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682048-C-T

93069023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682062-G-A

93069023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682062-G-T

93069340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682265-T-G

93069423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682348-C-T

93069490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682434-T-C

http://identifiers.org/hco/10/GRCh38#93069534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37682477-C-A

93069534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37682477-C-T