http://identifiers.org/hco/1/GRCh38#13583727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143026136-C-A

13583727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5 prime UTR variant
orthologous variants: 143026136-C-T

http://identifiers.org/hco/1/GRCh38#13583788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#143026083-C-A

13583788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 143026083-C-T

13583793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5 prime UTR variant
orthologous variants: 143026078-T-A

13583793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5 prime UTR variant
orthologous variants: 143026078-T-G

13583817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: synonymous_variant, undefined
orthologous variants: 143026054-G-A

13583817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: synonymous_variant, undefined
orthologous variants: 143026054-G-T

13583823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: synonymous variant
orthologous variants: 143026049-A-G

13583839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 143026033-A-G

13583845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 143026027-G-T

13583893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 143025975-G-A

13583893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 143025975-G-C

13584012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 143025830-G-A

13584012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 143025830-G-C

13584052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 143025805-C-T

13584112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025744-C-T

13584196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 143025668-A-G

13584196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 143025668-A-T

13584270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025636-G-A

13584270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025636-G-C

13584270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025636-G-T

http://identifiers.org/hco/1/GRCh38#13584277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#143025629-C-A

13584277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025629-C-G

13584330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025580-A-G

13584330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143025580-A-T

13584363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025544-C-T

13584371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025536-T-C

13584373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025534-G-A

13584373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025534-G-C

13584456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025478-G-C

13584456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025478-G-T

13584530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143025422-G-C

13584970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024784-C-G

13585013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024739-T-C

http://identifiers.org/hco/1/GRCh38#13585038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143024733-A-C

13585050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024723-C-T

13585068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024707-C-T

13585072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024703-C-T

13585121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024673-T-C

13585139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024655-G-A

http://identifiers.org/hco/1/GRCh38#13585336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143024528-C-A

13585336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024528-C-T

13585338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024526-G-A

13585375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024492-G-A

13585375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024492-G-T

13585506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143024331-A-G

13585562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143024283-C-G

13585562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143024283-C-T

13585588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143024265-C-T

13585742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024102-G-A

13585742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024102-G-C

13585742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024102-G-T

http://identifiers.org/hco/1/GRCh38#13585762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143024075-C-A

13585762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143024075-C-T

13585992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023905-T-C

13586024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023874-A-G

13586024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023874-A-T

13586117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023782-C-G

13586301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023594-G-T

13586382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023527-A-T

13586454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023456-A-G

13586520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023416-C-T

13587097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023139-G-A

13587097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143023139-G-T

13587874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143022094-C-T

13587941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021721-A-G

13588075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021603-G-T

13588126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021555-C-G

13588239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021438-C-T

13588241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021435-C-T

13588284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021393-A-G

13588284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021393-A-T

13588518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021203-A-G

13589069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143021104-C-T

13589332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143020248-A-G

13589389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143020187-A-G

13589463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143020113-G-A

13589463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143020113-G-T

13589559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143020020-C-T

13589594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143019985-G-T

13589654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143019940-A-G

http://identifiers.org/hco/1/GRCh38#13589695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143019879-A-C

http://identifiers.org/hco/1/GRCh38#13593253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143016132-C-A

13593253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143016132-C-T

13593260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143016126-G-C

13593570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143015737-G-A

13593851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143015496-C-T

13593949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143015391-C-T

13594124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143015214-G-A

13594155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143015196-C-G

13595549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143013211-G-A

13595549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143013211-G-T

http://identifiers.org/hco/1/GRCh38#13595713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143013066-C-A

13595769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143013034-C-G

13595772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143013031-G-A

http://identifiers.org/hco/1/GRCh38#13595794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143013007-C-A

13595794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143013007-C-G

http://identifiers.org/hco/1/GRCh38#13595810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143012990-C-A

13595810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143012990-C-T

13595831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 143012973-A-G

http://identifiers.org/hco/1/GRCh38#13595834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143012970-C-A

13595834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 143012970-C-T

13595874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 143012930-G-T

13596442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143012135-C-G

13596488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143012089-G-A

13596900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143011846-T-C

13596970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143011811-C-T

13597071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143011714-G-A

13603901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143006845-T-A

13604112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143006623-A-G

13604427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143006352-C-T

13604428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143006351-A-G

13604498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143006293-C-T

13604753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005672-T-C

13604796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005633-T-C

13604828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005628-C-T

13604929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005553-T-C

13605061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005396-G-A

13605117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005328-T-A

13605117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005328-T-C

13605346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005185-G-A

13605346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005185-G-T

http://identifiers.org/hco/1/GRCh38#13605347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143005184-C-A

13605349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005182-C-T

13605352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143005179-G-C

13605395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 143005144-G-A

13606428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143003611-G-A

13606438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143003601-G-A

13607047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143002883-A-G

http://identifiers.org/hco/1/GRCh38#13607053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143002877-C-A

13607053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143002877-C-G

13607103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143002845-A-G

13607274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 143002674-G-A

http://identifiers.org/hco/1/GRCh38#13607280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143002668-C-A

13607280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 143002668-C-G

13607280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 143002668-C-T

13607297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 143002648-G-A

13607297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 143002648-G-C

http://identifiers.org/hco/1/GRCh38#13607363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143002582-C-A

13607447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143002530-T-A

13607447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 143002530-T-C

http://identifiers.org/hco/1/GRCh38#13610393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#143000618-A-C

13610393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 143000618-A-G

13610440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 143000571-T-C

http://identifiers.org/hco/1/GRCh38#13611779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142998512-A-C

13613200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997567-T-C

13613239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997548-C-T

13613333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997453-C-T

13613379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997403-T-C

13613458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997338-A-G

13613575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997243-C-T

13613578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997240-G-T

http://identifiers.org/hco/1/GRCh38#13613599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142997219-C-A

13613599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997219-C-T

13613690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142997126-A-G

13613690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant, stop_gained
orthologous variants: 142997126-A-T

13613702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142997114-A-G

13613702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142997114-A-T

http://identifiers.org/hco/1/GRCh38#13613703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142997113-C-A

13613703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142997113-C-G

13613703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 142997113-C-T

13613794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997033-T-C

13613804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142997023-T-C

13613944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142996603-G-T

13613946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142996601-C-T

13614207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995964-A-G

13614207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995964-A-T

13614339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142995828-G-A

13614375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142995792-T-C

13614380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142995787-G-A

13614388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142995779-G-A

http://identifiers.org/hco/1/GRCh38#13614428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142995740-C-A

13614428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142995740-C-G

13614428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142995740-C-T

13614434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142995734-T-A

13614434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142995734-T-C

http://identifiers.org/hco/1/GRCh38#13615014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142995557-C-A

13615014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995557-C-T

13615052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995499-T-C

13615055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995496-A-G

13615082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995470-C-T

13615126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995413-G-A

13615144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995391-C-T

13615739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995152-G-A

http://identifiers.org/hco/1/GRCh38#13615770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142995129-C-A

13615793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995102-G-A

13615793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995102-G-C

13615793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995102-G-T

13615876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995016-A-G

http://identifiers.org/hco/1/GRCh38#13615895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142995004-A-C

13615895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142995004-A-G

13615979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994921-T-A

13615979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994921-T-G

http://identifiers.org/hco/1/GRCh38#13615987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994913-C-A

13615987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994913-C-T

13616016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994878-T-C

13616020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994874-C-T

http://identifiers.org/hco/1/GRCh38#13616025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994869-C-A

13616027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994867-A-G

13616037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994858-C-T

13616047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994848-T-C

http://identifiers.org/hco/1/GRCh38#13616050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994845-C-A

13616050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994845-C-T

http://identifiers.org/hco/1/GRCh38#13616079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994815-C-A

13616079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994815-C-G

13616079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994815-C-T

http://identifiers.org/hco/1/GRCh38#13616188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994704-C-A

13616188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994704-C-T

13616218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994694-A-T

http://identifiers.org/hco/1/GRCh38#13616220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994692-C-A

13616220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994692-C-G

13616243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994674-T-A

13616243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994674-T-C

13616243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994674-T-G

http://identifiers.org/hco/1/GRCh38#13616248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994669-A-C

13616248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994669-A-G

13616248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142994669-A-T

http://identifiers.org/hco/1/GRCh38#13616256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994662-C-A

13616325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994596-G-T

13616678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994447-T-C

13616686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994437-T-C

13616686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994437-T-G

13616688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994435-A-G

13616780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994359-C-T

13616873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994274-T-C

13616878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994269-T-A

http://identifiers.org/hco/1/GRCh38#13616925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#142994226-C-A

13616925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994226-C-G

13617907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29602
most severe consequence: 3 prime UTR variant
orthologous variants: 142994050-G-A