32105894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763638-A-G

32105903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763629-A-G

http://identifiers.org/hco/3/GRCh38#32105953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114763592-A-C

32105953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763592-A-G

32105972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763574-G-T

32106039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763490-T-C

32106047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763482-C-T

32106268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron_variant, undefined
orthologous variants: 114763285-G-A

http://identifiers.org/hco/3/GRCh38#32106369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#114763189-C-A

32106404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763157-T-C

32106404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763157-T-G

http://identifiers.org/hco/3/GRCh38#32106414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114763147-C-A

32106414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763147-C-G

32106414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763147-C-T

32106471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763096-G-A

32106471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763096-G-C

32106471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763096-G-T

http://identifiers.org/hco/3/GRCh38#32106545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114763023-C-A

32106545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114763023-C-T

32106581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114762987-G-A

32106581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114762987-G-C

32106581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron variant
orthologous variants: 114762987-G-T

32106664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762906-G-A

32106664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762906-G-T

32106701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762794-T-A

32106701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762794-T-C

32106772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762723-G-A

32106772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762723-G-T

http://identifiers.org/hco/3/GRCh38#32106805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114762690-C-A

32106805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762690-C-G

32106805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114762690-C-T

http://identifiers.org/hco/3/GRCh38#32106858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114762635-C-A

32106858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762635-C-T

32106885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762605-G-A

32106885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762605-G-T

http://identifiers.org/hco/3/GRCh38#32106943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114762549-C-A

32106943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762549-C-G

32106943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762549-C-T

http://identifiers.org/hco/3/GRCh38#32106959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#114762533-C-A

32106959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114762533-C-T

32107053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114762452-T-C

32107248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762269-C-T

32107280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762237-A-G

32107280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762237-A-T

32107332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762194-C-T

32107338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114762190-G-A

32107599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114761976-G-C

32107917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114761710-G-A

32109216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114760262-T-C

32109336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114760036-T-C

32109454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114759920-C-T

32110066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114758779-C-T

32110353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114758538-T-C

32114460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114754974-T-C

http://identifiers.org/hco/3/GRCh38#32114546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114754897-A-C

32114608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114754855-G-A

32115529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114754807-T-G

http://identifiers.org/hco/3/GRCh38#32119709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#114753509-C-A

32119750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114753461-C-T

32119883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114753337-T-C

32119883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114753337-T-G

32122490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114750554-C-T

32122592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114750452-A-G

32122592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114750452-A-T

32122692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114750407-C-T

32127893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749919-C-T

http://identifiers.org/hco/3/GRCh38#32127945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114749871-C-A

32127945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749871-C-G

32127945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749871-C-T

http://identifiers.org/hco/3/GRCh38#32128053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114749783-C-A

32128053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749783-C-G

32128063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749780-A-G

32128137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114749704-A-G

32128185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114749656-A-G

32128267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749571-G-A

32128267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749571-G-T

32128279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749559-T-C

32128280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749558-T-C

http://identifiers.org/hco/3/GRCh38#32128292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114749546-C-A

32128292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749546-C-T

32128304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749534-G-A

32128304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114749534-G-T

32130125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114748059-C-T

32130162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114748029-G-A

32130170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114748021-G-A

32138562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746214-G-A

32138562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746214-G-T

32138563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746213-G-A

32138611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114746163-G-T

32138620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114746154-G-T

32138623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114746151-G-A

32138671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 114746103-T-G

32138734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114746040-C-G

32138734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114746040-C-T

32138738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746037-T-A

32138757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746018-G-C

32138767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746011-A-T

32138768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114746010-T-A

32140168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114743585-T-C

http://identifiers.org/hco/3/GRCh38#32140174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114743579-A-C

32140200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114743558-C-T

32140203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114743555-T-A

32140203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114743555-T-C

32140209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114743549-C-T

32140210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114743548-T-C

32140246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 114743512-G-A

32140352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 114743406-G-A

32140374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114743385-C-G

32144254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114742509-T-A

32144254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114742509-T-C

32146639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 114740037-A-G

32146702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 114739974-G-A

32146702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 114739974-G-T

32147851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736673-A-G

32147977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736555-G-A

32148213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736326-C-T

32148243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736296-C-G

32148281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736267-G-A

32148285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736263-G-C

32148405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736173-A-G

32148549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114736053-A-G

32153955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114735722-T-C

32154015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114735665-A-G

32154167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114735584-T-C

32157886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114734849-C-T

32158062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114734667-C-T

32158339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734487-T-A

32158366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734459-T-C

32158366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734459-T-G

32158374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734451-G-T

32158386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734436-G-A

32158386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734436-G-C

32158386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734436-G-T

32158409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734413-G-T

32158411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734411-A-G

32158412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734410-G-A

32158412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734410-G-T

http://identifiers.org/hco/3/GRCh38#32158451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114734380-A-C

32158451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734380-A-G

32158590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734219-T-C

32158750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734168-T-G

32158757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734161-T-C

32158766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734160-G-A

32158766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734160-G-T

http://identifiers.org/hco/3/GRCh38#32158779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114734147-C-A

http://identifiers.org/hco/3/GRCh38#32158794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114734132-C-A

32158794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734132-C-G

32158794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734132-C-T

http://identifiers.org/hco/3/GRCh38#32158839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114734107-C-A

32158841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734106-G-A

32158841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114734106-G-T

32158906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114734044-G-A

32158975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114733975-T-C

32159032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114733918-G-A

32159032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114733918-G-C

http://identifiers.org/hco/3/GRCh38#32159127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114733838-C-A

32159127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114733838-C-T

http://identifiers.org/hco/3/GRCh38#32159131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114733834-C-A

32159131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114733834-C-T

http://identifiers.org/hco/3/GRCh38#32159146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114733819-C-A

32159201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114733750-A-G

32159205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114733746-T-A

32159557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114732844-T-C

32159560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114732841-T-C

32159631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114732770-G-T

http://identifiers.org/hco/3/GRCh38#32159651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114732750-C-A

32159651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114732750-C-G

http://identifiers.org/hco/3/GRCh38#32159799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114732626-C-A

32159799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114732626-C-G

32165809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114731578-A-G

32166118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114731279-G-C

32166118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114731279-G-T

32166227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114731126-G-A

32166227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114731126-G-C

32166227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114731126-G-T

http://identifiers.org/hco/3/GRCh38#32166320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114731024-A-C

32166320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114731024-A-G

32166429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730935-T-C

32166528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730846-A-G

http://identifiers.org/hco/3/GRCh38#32166812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114730608-C-A

http://identifiers.org/hco/3/GRCh38#32166881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114730551-C-A

32166881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730551-C-T

32166918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730515-A-G

32166938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730505-A-G

http://identifiers.org/hco/3/GRCh38#32166970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114730463-C-A

32166970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730463-C-T

32167033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730424-G-T

32167112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730334-A-G

32167275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730176-G-A

32167295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730161-G-T

32167316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114730140-C-T

32167492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729931-T-C

32167655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729789-A-T

32167671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729773-C-T

32167684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729760-T-C

32167804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729633-T-G

32167862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729586-A-G

32167865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729583-A-G

http://identifiers.org/hco/3/GRCh38#32167906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114729542-A-C

32167906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729542-A-G

32168057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729402-G-T

32168086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729375-A-G

http://identifiers.org/hco/3/GRCh38#32168146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114729306-C-A

http://identifiers.org/hco/3/GRCh38#32168262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114729213-C-A

32168262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729213-C-T

32168427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729085-A-G

http://identifiers.org/hco/3/GRCh38#32168433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114729079-C-A

32168433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729079-C-T

32168436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114729076-T-C

32168649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28956
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114728904-A-T