71671298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99591029-C-T

71671347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99591078-G-A

71672826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99592544-G-A

71673347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99593025-A-G

71673911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99593984-A-T

71674640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99594393-T-C

71674700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99594447-T-A

http://identifiers.org/hco/3/GRCh38#71674782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99594504-A-C

71674867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99594585-T-G

71675085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99594765-T-C

71675466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99595143-T-C

71675927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99595995-T-A

71676062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99596098-T-C

71676135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99596180-C-T

71676733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99596348-G-A

71676733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99596348-G-C

71677110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99596680-A-G

71677418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597017-T-C

71677418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597017-T-G

http://identifiers.org/hco/3/GRCh38#71677541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99597130-C-A

71677575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597166-T-C

71677589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597177-A-G

71677643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597232-T-C

71677644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597233-T-A

http://identifiers.org/hco/3/GRCh38#71677728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99597314-C-A

71677728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597314-C-T

71677772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597361-T-A

http://identifiers.org/hco/3/GRCh38#71677792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99597380-C-A

71677792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597380-C-T

71677814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597402-C-G

71677814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597402-C-T

71678089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597644-T-C

71678249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597853-A-G

71678269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99597873-T-A

71678429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598047-C-G

71678440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598058-T-C

71678937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598582-T-C

71678937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598582-T-G

71679020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598668-T-C

71679090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598737-T-C

71679116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598760-G-T

71679246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598898-T-A

71679246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99598898-T-C

http://identifiers.org/hco/3/GRCh38#71679291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99598937-C-A

71679655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599273-T-C

71679722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599342-C-G

http://identifiers.org/hco/3/GRCh38#71680009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99599631-C-A

71680070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599646-G-T

71680084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599660-A-G

71680319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599864-T-A

71680319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599864-T-C

71680333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599878-T-C

71680333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599878-T-G

71680343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599887-A-G

71680393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99599937-G-T

71680594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99600115-T-C

71680594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99600115-T-G

71680604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99600129-A-G

http://identifiers.org/hco/3/GRCh38#71680729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99600243-C-A

71681124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99600535-A-G

71681438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99600827-T-C

71681521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99600902-G-A

71681521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99600902-G-T

http://identifiers.org/hco/3/GRCh38#71681537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99600917-C-A

http://identifiers.org/hco/3/GRCh38#71682205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99601571-C-A

71682859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602233-T-C

71683104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602462-A-G

71683105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602463-G-C

71683145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602499-G-A

71683383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602710-C-G

71683383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602710-C-T

71683435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602744-G-A

71683691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99602960-T-C

71683804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603056-C-T

http://identifiers.org/hco/3/GRCh38#71683909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99603151-C-A

71683909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603151-C-T

71683996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603251-T-C

71684270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603499-G-A

71684270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603499-G-T

71684272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603501-T-G

71684332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603555-T-C

71684511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603795-T-C

http://identifiers.org/hco/3/GRCh38#71684523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99603807-A-C

71684523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99603807-A-G

http://identifiers.org/hco/3/GRCh38#71684549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99603834-C-A

71685009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99604296-G-A

71685009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99604296-G-C

71685022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99604309-T-C

71685094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99604375-G-A

71685679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99604603-A-G

71685753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99604665-C-T

71687448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99606792-T-C

71687517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99606864-G-A

71687525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99606875-G-A

71687782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99607110-T-C

71687868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99607178-T-C

http://identifiers.org/hco/3/GRCh38#71688495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99607781-C-A

71688648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99607905-C-T

71689353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99608584-T-A

71689353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99608584-T-C

71689367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99608598-C-T

http://identifiers.org/hco/3/GRCh38#71689869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99609075-C-A

71689869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609075-C-G

71689869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609075-C-T

http://identifiers.org/hco/3/GRCh38#71689878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99609084-A-C

71689878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609084-A-G

71689878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609084-A-T

71689909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609118-T-A

71689909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609118-T-C

71689929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609138-A-G

71690144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99609352-C-T

http://identifiers.org/hco/3/GRCh38#71690161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99609369-A-C

http://identifiers.org/hco/3/GRCh38#71690185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99609393-A-C

71690277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609465-A-G

71690290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609467-T-A

71690290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609467-T-C

71690295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609472-T-A

71690318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609495-G-A

71690640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609820-C-T

71690684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99609860-G-A

http://identifiers.org/hco/3/GRCh38#71690704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99609880-C-A

71690889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99610036-T-C

http://identifiers.org/hco/3/GRCh38#71690968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99610098-C-A

71690993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99610113-C-T

71691179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99610298-T-C

71691179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99610298-T-G

http://identifiers.org/hco/3/GRCh38#71691736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99610820-C-A

71692043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99611065-T-C

71692137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99611140-G-C

71692322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99611317-T-C

71692471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99611396-G-A

71692518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99611443-T-A

71693637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99612434-A-G

71693697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99612899-C-T

71693749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99612949-T-C

http://identifiers.org/hco/3/GRCh38#71693844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99613042-C-A

71693844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613042-C-G

71693844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613042-C-T

71693947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99613142-A-G

71693986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613172-T-C

http://identifiers.org/hco/3/GRCh38#71694062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99613226-C-A

71694062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613226-C-T

71694096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613250-C-T

71694102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613256-C-T

71694126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613270-T-C

71694161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613312-G-A

71694341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613480-T-C

71694526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613666-A-T

71694547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613687-C-T

71694661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613812-C-T

71694672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613823-T-C

71694703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99613845-A-G

http://identifiers.org/hco/3/GRCh38#71695146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99614237-C-A

http://identifiers.org/hco/3/GRCh38#71695223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99614320-A-C

71695338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99614420-T-C

http://identifiers.org/hco/3/GRCh38#71695722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99614863-C-A

71696143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99615620-G-T

71696309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616014-A-G

71696309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616014-A-T

71696321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616026-T-C

71696321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616026-T-G

71696328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616033-A-T

71696549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616213-C-T

71696563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616228-T-A

71696564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616229-G-T

71698237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616392-T-G

71698267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616422-C-T

71698408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616553-T-A

http://identifiers.org/hco/3/GRCh38#71698463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99616596-A-C

71698483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616615-G-A

71698658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616760-A-T

71698715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99616796-A-G

71699353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617326-A-G

71699424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617387-G-A

71699429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617395-T-G

71699522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617479-G-T

71699586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617549-G-T

71699601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617564-G-A

71699601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617564-G-T

71699605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617568-G-A

71699825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617793-A-G

71699829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617797-T-C

71699829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617797-T-G

71699834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99617802-T-G

71700696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620039-G-A

71701778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620324-A-G

http://identifiers.org/hco/3/GRCh38#71701788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99620332-A-C

71701829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620377-A-G

71701833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620381-T-C

71701964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620505-G-T

71701987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620531-T-C

http://identifiers.org/hco/3/GRCh38#71701991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99620535-A-C

71702005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620548-G-C

71702095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620617-A-G

71702127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620650-A-G

71702184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620709-A-G

71702408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620930-C-T

71702410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620932-G-A

71702413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99620935-C-T

71702523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99621048-A-G

71702711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99621223-T-A

http://identifiers.org/hco/3/GRCh38#71702743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99621246-C-A

71703030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99621475-T-G

http://identifiers.org/hco/3/GRCh38#71703793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99622344-C-A

71703793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99622344-C-G

71703793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99622344-C-T

71704462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99623914-G-A

http://identifiers.org/hco/3/GRCh38#71704484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99623936-C-A

71704495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99623947-C-T

http://identifiers.org/hco/3/GRCh38#71704558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99624005-A-C

71704626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99624081-T-C

71704758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99624183-C-G

71704919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99624354-T-C

71706800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99625813-G-A

http://identifiers.org/hco/3/GRCh38#71707393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99626349-C-A

71707408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99626361-T-C

71707633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99626536-G-T

71707794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99626690-T-C

71707819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99626707-G-A

71708233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99626826-T-C

71708445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99626987-T-C

http://identifiers.org/hco/3/GRCh38#71708563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99627101-C-A

71708563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627101-C-G

71708563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627101-C-T

http://identifiers.org/hco/3/GRCh38#71708669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99627191-A-C

71708736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627270-T-C

71708736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627270-T-G

http://identifiers.org/hco/3/GRCh38#71708944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99627481-C-A

71708998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627534-T-C

71708998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627534-T-G

71709249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99627715-T-C

http://identifiers.org/hco/3/GRCh38#71709269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99627735-C-A

71710278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628556-A-T

71710391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628660-T-C

http://identifiers.org/hco/3/GRCh38#71710549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99628816-C-A

71710565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628832-A-G

71710574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628866-T-A

71710574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628866-T-C

http://identifiers.org/hco/3/GRCh38#71710581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99628898-C-A

71710584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628901-G-T

71710618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99628938-C-G

71710809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629118-T-C

71710919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629229-T-C

71710948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629257-A-G

71711154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629453-G-A

71711157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629456-A-G

71711244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629561-T-C

71711266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99629583-T-C

http://identifiers.org/hco/3/GRCh38#71711427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99629739-C-A

http://identifiers.org/hco/3/GRCh38#71711593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99629912-C-A

71711777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630134-G-C

http://identifiers.org/hco/3/GRCh38#71711999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99630316-C-A

71712203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630528-T-C

71712268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630577-T-C

71712345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630652-C-T

71712635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630952-T-A

71712635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630952-T-C

71712635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630952-T-G

http://identifiers.org/hco/3/GRCh38#71712659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99630968-A-C

71712665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99630974-A-G

71712779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99631086-A-G

71712810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99631116-T-A

71712918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99631211-T-G

http://identifiers.org/hco/3/GRCh38#71713143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99631404-C-A

71713206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99631464-C-T

http://identifiers.org/hco/3/GRCh38#71713290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99631550-C-A

71713297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99631557-G-A

71713365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99632395-T-A

71714544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99633129-C-T

71715100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99633850-C-G

71715713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99634419-C-T

71716784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99635805-T-C

http://identifiers.org/hco/3/GRCh38#71716894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99635877-C-A

71717060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99635987-C-T

71717181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99636108-C-T

71717311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99636233-C-T

71717478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99636402-G-A

71717524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99636842-T-C

71717735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99637039-G-A

71717741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99637045-T-C

71717891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99637184-T-C

71717980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99637265-A-G

71718392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99637647-G-A

71719221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99638513-T-G

http://identifiers.org/hco/3/GRCh38#71719340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99638631-A-C

71719432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99638721-G-A

http://identifiers.org/hco/3/GRCh38#71719541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99638830-A-C

http://identifiers.org/hco/3/GRCh38#71721211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99640386-C-A

71721211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99640386-C-T

71721212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99640387-G-A

71722117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99640542-T-A

71722130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99640555-T-C

71722517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99640901-G-A

71722629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99641006-C-G

71722887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99641469-T-C

71723559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99642315-G-A

71723559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99642315-G-C

http://identifiers.org/hco/3/GRCh38#71723570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99642330-C-A

71723570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99642330-C-T

71723939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99642683-G-A

http://identifiers.org/hco/3/GRCh38#71723952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99642696-C-A

71724319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99643054-G-T

71725048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99643527-G-A

71725048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99643527-G-C

71725048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99643527-G-T

http://identifiers.org/hco/3/GRCh38#71725242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99643639-A-C

71725242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99643639-A-G

71725242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99643639-A-T

71725305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99643666-G-A

71725305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99643666-G-C

71725305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99643666-G-T

71725349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99643695-C-T

71725374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99643720-C-T

71725607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99643845-G-T

71726136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99644282-A-T

71726280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99644403-A-G

71726666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99644695-A-G

71726676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99644705-G-T

71726703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99644731-C-T

71726753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99644773-G-A

71727082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99645073-A-G

71727197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99645182-C-G

http://identifiers.org/hco/3/GRCh38#71727616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99645554-A-C

71727616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99645554-A-G

71727945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99645861-T-A

71728037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99645938-A-G

71728108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99646008-A-G

71728235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99646132-G-C

71728363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99646273-C-T

71728626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 99646531-A-G

71728694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99646599-T-C

71728699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99646604-T-C

http://identifiers.org/hco/3/GRCh38#71728709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99646614-C-A

71728766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99646671-G-A

71728766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99646671-G-T

71728797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99646702-C-T

71729000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99646908-G-T

71729045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99646982-G-A

71729045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99646982-G-T

http://identifiers.org/hco/3/GRCh38#71729209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99647148-C-A

71729209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, undefined
orthologous variants: 99647148-C-T

71729254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647193-G-A

71729254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647193-G-T

http://identifiers.org/hco/3/GRCh38#71729257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99647196-A-C

http://identifiers.org/hco/3/GRCh38#71729312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99647248-C-A

71729314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647250-C-G

71729314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647250-C-T

71729345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647279-T-C

71729390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647320-G-T

71729586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, undefined
orthologous variants: 99647602-C-T

71729608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, undefined
orthologous variants: 99647618-G-T

71729618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99647628-A-T

71729850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, undefined
orthologous variants: 99647816-T-A

71729850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, undefined
orthologous variants: 99647816-T-G

71731094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99648463-C-T

71731192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99648537-C-T

71731207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99648575-G-T

71731498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99648878-T-C

71731589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99648944-G-A

71731693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99649023-C-T

71731793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99649104-T-A

71731861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99649171-T-C

http://identifiers.org/hco/3/GRCh38#71732216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99649515-C-A

71733735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99650320-A-G

71733737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99650322-T-C

71734068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99650662-T-G

71734126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99650715-T-A

http://identifiers.org/hco/3/GRCh38#71734869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99651441-C-A

71734924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99651495-T-C

71735233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99651792-C-T

71735282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99651841-C-T

71735380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99651939-G-A

71735428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99651997-G-A

71735516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99652083-C-T

71736068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99652935-A-T

71736189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99653033-G-A

http://identifiers.org/hco/3/GRCh38#71736222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99653063-C-A

http://identifiers.org/hco/3/GRCh38#71736452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99653243-A-C

71737148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654216-C-T

71737327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654397-C-T

71737329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654399-G-A

71737331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654401-G-A

71737331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654401-G-C

http://identifiers.org/hco/3/GRCh38#71737433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99654491-C-A

71737433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654491-C-T

71737737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654756-G-A

71737834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654847-A-G

71737970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99654991-C-T

http://identifiers.org/hco/3/GRCh38#71738011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99655015-A-C

71738292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99655297-C-T

http://identifiers.org/hco/3/GRCh38#71746592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99664500-C-A

71746592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99664500-C-T

71746644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99664537-G-A

71749245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99665574-G-A

71749328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99665621-C-T

http://identifiers.org/hco/3/GRCh38#71749409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99665689-C-A

71749452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99665732-G-C

71749820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99666025-T-C

71749820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99666025-T-G

71749900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99666091-T-C

71750163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99666401-T-C

71750348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99666581-T-C

71751333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99667094-C-T

71751429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99667192-C-G

71751968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99667616-C-T

71751973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99667621-C-T

71752159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99667786-C-G

71752364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99668073-G-A

71752469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99668168-A-G

71752590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99668252-T-G

71752734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99668394-A-G

71752734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99668394-A-T

http://identifiers.org/hco/3/GRCh38#71753416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99669033-C-A

71753416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669033-C-T

http://identifiers.org/hco/3/GRCh38#71753448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99669075-C-A

71753448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669075-C-T

71753689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669309-G-A

71753689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669309-G-C

71753689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669309-G-T

http://identifiers.org/hco/3/GRCh38#71753695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99669315-C-A

71753695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669315-C-G

71753695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron variant
orthologous variants: 99669315-C-T

71753921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99669532-G-A

71753921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99669532-G-T

71754013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99669615-G-A

71754013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99669615-G-C

71754013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99669615-G-T

http://identifiers.org/hco/3/GRCh38#71754097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99669696-C-A

71754097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99669696-C-G

71754097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99669696-C-T

71754356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 99669955-G-A

71754356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 99669955-G-C

71754356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 99669955-G-T

http://identifiers.org/hco/3/GRCh38#71754376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99669975-C-A

71754376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 99669975-C-T

http://identifiers.org/hco/3/GRCh38#71754532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99670131-C-A

71754532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, missense_variant
orthologous variants: 99670131-C-G

71754532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99670131-C-T

71754694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 99670296-G-A

71754694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 99670296-G-C

71754694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31837
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 99670296-G-T