14125034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91450703-G-A

14125034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91450703-G-T

14125096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450770-G-A

14125096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450770-G-T

14125102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450778-G-T

14125120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450796-G-C

14125120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450796-G-T

http://identifiers.org/hco/3/GRCh38#14125126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91450802-A-C

14125159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450835-C-G

14125159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450835-C-T

14125185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 91450861-G-T

14125255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 91450918-T-A

14125255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 91450918-T-C

14125262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 91450926-T-C

14125342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91450968-T-A

14125352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91450978-T-A

14125352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91450978-T-C

14125352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91450978-T-G

14126029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451563-C-T

14126055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451589-G-A

http://identifiers.org/hco/3/GRCh38#14126158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91451678-C-A

14126158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451678-C-T

14126216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451723-C-T

14126339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451807-G-T

14126424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451876-T-C

14126427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451879-C-T

14126476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91451934-G-A

14126641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91452079-A-G

14126722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91452143-C-G

14126892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91452635-G-A

14127466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453003-G-A

14127552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453070-G-T

14127572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453089-G-T

14127585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453102-C-T

http://identifiers.org/hco/3/GRCh38#14127917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91453418-A-C

14128014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453515-C-G

14128014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453515-C-T

14128032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453534-C-T

14128195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453645-A-G

14128308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453740-C-G

14128453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453841-T-C

14128612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91453975-T-C

14128747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91454093-T-C

14128752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91454098-G-A

http://identifiers.org/hco/3/GRCh38#14128776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91454122-A-C

14129478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 91454293-G-T

14130368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91454819-G-T

14130530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91454959-A-T

14130591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455024-G-A

14130845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91455211-C-G

14130845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91455211-C-T

14130976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455332-C-T

14131026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455361-T-C

14131030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455365-A-G

14131084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455391-T-A

14131097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455404-G-C

14131097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455404-G-T

14131515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455625-C-T

http://identifiers.org/hco/3/GRCh38#14131532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91455642-C-A

14131532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455642-C-G

14131532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455642-C-T

14131539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455649-G-A

14131539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455649-G-T

14131685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455793-G-C

14131689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455799-T-A

14131740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455841-A-G

14131740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455841-A-T

http://identifiers.org/hco/3/GRCh38#14131790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91455895-C-A

14131790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91455895-C-T

14131998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456047-T-C

14132043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456077-T-A

14132078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456127-G-T

14132101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456150-G-A

14132152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456199-T-C

14132157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456204-T-C

14132200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456246-G-A

14132221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456260-C-T

14132378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456409-T-G

14132398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456423-T-C

14132481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456492-G-A

14132481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456492-G-T

http://identifiers.org/hco/3/GRCh38#14132615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91456645-C-A

14132615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456645-C-T

14132647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456676-G-A

14132704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456717-C-T

http://identifiers.org/hco/3/GRCh38#14132721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91456724-A-C

14132721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456724-A-G

14132793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456807-G-A

14132826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456821-C-T

14132915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91456912-G-A

14132915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 91456912-G-C

http://identifiers.org/hco/3/GRCh38#14132988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91456982-C-A

14132988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91456982-C-T

http://identifiers.org/hco/3/GRCh38#14133034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91457030-C-A

14133034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457030-C-T

14133059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457058-T-G

14133169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457140-C-T

14133621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457538-G-A

14133621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457538-G-C

14133621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457538-G-T

14133655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457559-A-G

14133799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 91457692-C-T

14133903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457806-G-T

http://identifiers.org/hco/3/GRCh38#14133920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91457829-C-A

14133920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457829-C-T

14134006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457897-C-T

14134007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457898-A-G

14134077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91457970-C-T

14134489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458322-G-A

14134489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458322-G-T

14134534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458366-T-G

14134624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458473-G-A

14134624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458473-G-T

14134655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458506-G-A

14134655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458506-G-T

14134735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458879-G-A

14134735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458879-G-T

14134761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458905-T-A

14134761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91458905-T-G

14134765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 91458909-C-T

14135171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 91459249-G-A

14135171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 91459249-G-C

14135171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 91459249-G-T

14135330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459387-T-C

14135330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459387-T-G

14135670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459510-G-A

14135670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459510-G-C

14135670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459510-G-T

http://identifiers.org/hco/3/GRCh38#14135722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91459556-C-A

14135722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459556-C-G

14135722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459556-C-T

http://identifiers.org/hco/3/GRCh38#14135953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91459775-C-A

14135953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459775-C-T

http://identifiers.org/hco/3/GRCh38#14135965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91459788-C-A

14135965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459788-C-T

14136015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459819-A-G

14136143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459872-G-A

14136519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91459991-G-A

14136928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460328-G-T

14136997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460393-G-A

14136997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460393-G-T

14137006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460402-A-G

14137078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460470-G-A

14137078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460470-G-T

14137119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460512-G-T

http://identifiers.org/hco/3/GRCh38#14137324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91460720-A-C

http://identifiers.org/hco/3/GRCh38#14137329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91460725-A-C

14137329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460725-A-G

14137331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460727-G-A

14137331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460727-G-T

14137456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91460846-G-A

http://identifiers.org/hco/3/GRCh38#14137787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91461062-C-A

14137815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91461081-T-C

14137823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91461090-T-C

14137997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91461202-T-A

14138343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91461474-G-A

14138756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91461888-G-A

14139062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462209-G-A

14139062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462209-G-T

14139109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462244-A-G

http://identifiers.org/hco/3/GRCh38#14139162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91462281-C-A

14139331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462453-T-C

14139359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462469-T-A

14139377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462491-T-C

14139386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462500-A-G

http://identifiers.org/hco/3/GRCh38#14139421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91462533-C-A

14139421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462533-C-T

http://identifiers.org/hco/3/GRCh38#14139435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91462547-C-A

14139435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462547-C-T

http://identifiers.org/hco/3/GRCh38#14139447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91462563-C-A

14140092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462958-C-T

http://identifiers.org/hco/3/GRCh38#14140093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91462959-A-C

14140093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91462959-A-G

14140300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91463161-T-G

14140422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 91463258-G-A

http://identifiers.org/hco/3/GRCh38#14141711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91463845-C-A

14141778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 91463912-G-A

http://identifiers.org/hco/3/GRCh38#14141857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91463959-C-A

14141857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91463959-C-G

14141896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91463977-T-C

http://identifiers.org/hco/3/GRCh38#14141907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91463988-C-A

14141907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91463988-C-T

http://identifiers.org/hco/3/GRCh38#14141923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91464003-C-A

14141923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464003-C-G

14141923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464003-C-T

14142011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464038-G-T

http://identifiers.org/hco/3/GRCh38#14142101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91464076-C-A

14142148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464100-T-C

http://identifiers.org/hco/3/GRCh38#14142221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91464169-C-A

14142239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464187-T-A

14142239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464187-T-C

14142239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464187-T-G

http://identifiers.org/hco/3/GRCh38#14142250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91464198-C-A

14142250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464198-C-G

14142250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464198-C-T

14142251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464199-G-A

14142251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464199-G-T

14142275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464223-G-A

14142275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464223-G-C

14142275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464223-G-T

http://identifiers.org/hco/3/GRCh38#14142298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91464247-A-C

14142316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464263-G-A

14142440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464339-G-A

14142503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464391-C-T

14142573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464435-A-G

14142627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464465-T-C

14142670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464502-T-A

14142755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464572-G-A

http://identifiers.org/hco/3/GRCh38#14142896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91464711-C-A

14142980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464788-T-C

14143013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464821-G-A

14143013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464821-G-C

14143013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464821-G-T

14143128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91464936-C-T

http://identifiers.org/hco/3/GRCh38#14143291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91465079-A-C

14143291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91465079-A-T

14143300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91465088-C-G

14143314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91465104-A-G

14143414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91465189-A-G

14143610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28472
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 91465372-C-G