http://identifiers.org/hco/10/GRCh38#49734696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32070051-A-C

49734696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32070051-A-G

49734696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32070051-A-T

http://identifiers.org/hco/10/GRCh38#49734793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32070003-C-A

49734816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32069981-T-C

http://identifiers.org/hco/10/GRCh38#49734861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32069938-A-C

49734861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32069938-A-G

http://identifiers.org/hco/10/GRCh38#49734959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32069832-C-A

49734959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32069832-C-T

49735103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32069643-T-C

49735179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32069598-T-A

http://identifiers.org/hco/10/GRCh38#49735186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32069597-C-A

49735186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32069597-C-T

http://identifiers.org/hco/10/GRCh38#49735343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32069469-C-A

49735432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069422-G-A

49735432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069422-G-C

49735432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069422-G-T

49735433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069421-G-A

49735433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069421-G-T

49735459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069395-G-A

49735459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069395-G-T

49735482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069373-G-T

49735560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069315-G-A

49735661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069243-G-A

49735864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069042-T-C

http://identifiers.org/hco/10/GRCh38#49735877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068962-C-A

49735877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068962-C-G

49735877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068962-C-T

49735889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068949-T-C

49735952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068897-T-C

49735975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068860-A-T

http://identifiers.org/hco/10/GRCh38#49736206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068625-C-A

49736206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068625-C-T

49736211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068621-G-A

49736211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068621-G-C

49736222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068610-A-G

http://identifiers.org/hco/10/GRCh38#49736276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068580-C-A

49736276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068580-C-T

49736382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32068491-T-A

49736406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32068467-C-T

49736548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068325-G-A

49736548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068325-G-T

49736567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068306-C-G

49736567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068306-C-T

http://identifiers.org/hco/10/GRCh38#49736579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068294-A-C

49736579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068294-A-G

http://identifiers.org/hco/10/GRCh38#49736582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068291-A-C

49736616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068259-T-A

http://identifiers.org/hco/10/GRCh38#49736621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068255-C-A

http://identifiers.org/hco/10/GRCh38#49736629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068248-A-C

49736629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068248-A-G

49736635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068243-G-A

49736635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068243-G-T

49736653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068228-G-A

49736653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068228-G-T

http://identifiers.org/hco/10/GRCh38#49736809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32068084-A-C

49736823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068070-T-C

49736926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067956-C-T

49737050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067854-T-C

49737089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067818-G-A

49737704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067235-G-A

49737704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067235-G-T

http://identifiers.org/hco/10/GRCh38#49737712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32067227-C-A

49737712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067227-C-T

49737725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067214-G-A

49737725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067214-G-T

http://identifiers.org/hco/10/GRCh38#49737730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32067209-A-C

49737934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066992-G-A

http://identifiers.org/hco/10/GRCh38#49738123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066788-C-A

49738164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32066768-T-A

49738192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32066739-G-A

49738222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32066709-T-C

49738285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32066651-C-G

49738285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32066651-C-T

http://identifiers.org/hco/10/GRCh38#49739539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066548-C-A

49739539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32066548-C-T

49739551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066536-G-T

http://identifiers.org/hco/10/GRCh38#49739555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066532-C-A

49739555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066532-C-G

http://identifiers.org/hco/10/GRCh38#49739628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066469-C-A

49739855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066260-G-A

49739885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066232-G-T

49739926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066190-T-A

49739926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066190-T-C

http://identifiers.org/hco/10/GRCh38#49739927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066189-C-A

49739927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066189-C-T

49739948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066168-T-C

http://identifiers.org/hco/10/GRCh38#49739949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066166-C-A

http://identifiers.org/hco/10/GRCh38#49739951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32066164-C-A

49739973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066143-T-A

49739973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066143-T-C

49739973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066143-T-G

49739974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066142-T-C

49739984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066132-T-C

49740004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066112-T-C

http://identifiers.org/hco/10/GRCh38#49740536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065421-C-A

49740559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065398-G-A

49740559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065398-G-T

http://identifiers.org/hco/10/GRCh38#49740579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065378-C-A

49740579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065378-C-T

49740581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065376-A-G

http://identifiers.org/hco/10/GRCh38#49740602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065358-C-A

49740604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065356-G-T

http://identifiers.org/hco/10/GRCh38#49740628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065340-C-A

http://identifiers.org/hco/10/GRCh38#49740629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065339-C-A

49740629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065339-C-T

49740637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065328-G-A

49740637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065328-G-T

http://identifiers.org/hco/10/GRCh38#49740647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065320-C-A

49740733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32065262-G-C

49740767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32065228-G-A

49740908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065110-G-A

49740908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065110-G-T

http://identifiers.org/hco/10/GRCh38#49740966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065055-C-A

http://identifiers.org/hco/10/GRCh38#49740967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32065054-A-C

49740967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065054-A-T

http://identifiers.org/hco/10/GRCh38#49741054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064990-C-A

49741082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064964-C-G

49741186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064856-A-G

http://identifiers.org/hco/10/GRCh38#49741246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064800-C-A

49741492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064555-G-T

http://identifiers.org/hco/10/GRCh38#49741498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064552-A-C

49742685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064351-G-A

49742685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064351-G-C

49742685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064351-G-T

http://identifiers.org/hco/10/GRCh38#49742735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064306-C-A

49742735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064306-C-G

49742735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064306-C-T

http://identifiers.org/hco/10/GRCh38#49742736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064305-C-A

49742736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064305-C-G

49742736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064305-C-T

http://identifiers.org/hco/10/GRCh38#49742741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064300-C-A

49742741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064300-C-T

49742750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064298-G-A

49742750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064298-G-T

http://identifiers.org/hco/10/GRCh38#49742828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32064145-C-A

49743009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063977-A-G

49743078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063935-T-A

49743102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063908-G-A

49743102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063908-G-C

49743102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063908-G-T

49743114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063898-A-G

http://identifiers.org/hco/10/GRCh38#49743674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32063604-A-C

49743674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32063604-A-G

49743674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32063604-A-T

http://identifiers.org/hco/10/GRCh38#49743842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32063445-C-A

49743842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32063445-C-T

49743890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32063392-G-T

49744056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32063223-A-G

49744151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063131-T-C

http://identifiers.org/hco/10/GRCh38#49744177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32063099-C-A

http://identifiers.org/hco/10/GRCh38#49744226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32063052-C-A

http://identifiers.org/hco/10/GRCh38#49744227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32063051-C-A

49744227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063051-C-T

49744271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063019-A-G

49744450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062876-C-G

49744549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062784-T-C

49744617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062733-G-A

49744879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062482-T-C

49744893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062468-C-T

49745158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062192-C-T

49745211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062140-T-C

49745261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062092-A-G

49745315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062031-T-C

49745405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32061949-A-T

49745444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32061910-T-C

49745617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061759-T-C

http://identifiers.org/hco/10/GRCh38#49745651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32061724-C-A

49745651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061724-C-T

49745656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061719-C-T

http://identifiers.org/hco/10/GRCh38#49745697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32061675-C-A

49745697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061675-C-T

49745710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061664-G-A

49745710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061664-G-T

http://identifiers.org/hco/10/GRCh38#49745750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32061582-C-A

49745981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32061158-C-T

49746004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061135-G-A

49746006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061133-C-T

http://identifiers.org/hco/10/GRCh38#49746038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32061075-C-A

49746038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061075-C-T

49746094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060938-A-G

49746124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060908-A-G

49746159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060874-G-T

49746598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060035-G-T

http://identifiers.org/hco/10/GRCh38#49746653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32059930-C-A

49746653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059930-C-T

49746661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059922-C-T

49746683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059900-C-T

49746692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059891-G-A

49746692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059891-G-T

49746826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32059762-A-G

49746988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059597-T-G

49746989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059596-G-A

49747014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059591-C-G

http://identifiers.org/hco/10/GRCh38#49747016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32059589-C-A

49747016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059589-C-G

49747016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059589-C-T

49747020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059585-T-C

49747020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059585-T-G

49747069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32059536-T-A

49747090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32059515-G-C

http://identifiers.org/hco/10/GRCh38#49747332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32059333-C-A

49748185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32058731-T-C

49748416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32058540-A-T

http://identifiers.org/hco/10/GRCh38#49748431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32058525-A-C

49749573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32057504-C-T

49749576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32057501-G-A

49749576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32057501-G-T

49749667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32057432-A-G

http://identifiers.org/hco/10/GRCh38#49749807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32057299-C-A

49749807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32057299-C-G

49749807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32057299-C-T

49749858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056576-A-G

49749858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056576-A-T

49749859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056575-G-A

49749859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056575-G-T

49749860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056574-G-A

49749860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056574-G-T

http://identifiers.org/hco/10/GRCh38#49749891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32056544-C-A

49749894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056541-G-C

49749894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056541-G-T

http://identifiers.org/hco/10/GRCh38#49749895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32056540-C-A

49749895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056540-C-T

49749897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056538-T-A

49749926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056504-G-A

49749926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056504-G-T

http://identifiers.org/hco/10/GRCh38#49749929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32056501-C-A

http://identifiers.org/hco/10/GRCh38#49749956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32056465-C-A

49749956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056465-C-T

49750059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056368-G-A

49750076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056343-C-T

49750099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056320-C-T

49750299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056194-T-G

49750356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056187-G-A

49750642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055939-C-T

49750688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055893-G-A

49750688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055893-G-T

49750706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055875-G-T

http://identifiers.org/hco/10/GRCh38#49750723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32055872-C-A

49750808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055850-T-C

49750808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055850-T-G

49751000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055654-G-A

49751001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055653-A-G

49751016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055640-G-A

49751022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055634-G-C

49751022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055634-G-T

49751033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055623-G-C

http://identifiers.org/hco/10/GRCh38#49751115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32055542-C-A

49751115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055542-C-T

49751494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055185-G-T

49751617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055053-C-T

49751744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054927-T-C

49751744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054927-T-G

49752098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054591-C-T

49752106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054583-G-A

49752134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32054555-T-G

49752303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054431-A-G

49752379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054412-A-G

49752379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054412-A-T

49752385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054406-A-T

49752423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054376-C-T

49752602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054264-C-T

49752826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054068-T-C

49752835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054059-T-A

49752835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054059-T-C

http://identifiers.org/hco/10/GRCh38#49752849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32054045-C-A

49752849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054045-C-T

49752859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054035-T-C

49752859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054035-T-G

49752869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054026-G-A

49752869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054026-G-T

49752916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053993-G-A

49752982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053932-C-T

49753028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053818-A-G

49753064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053754-A-G

49753297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053478-T-A

49756452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049335-T-A

49756452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049335-T-C

49756452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049335-T-G

http://identifiers.org/hco/10/GRCh38#49756457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32049330-C-A

49756471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32049316-T-C

49756477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32049312-A-G

49756546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32049248-A-G

49756549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32049245-A-T

http://identifiers.org/hco/10/GRCh38#49756556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32049238-C-A

49756556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32049238-C-T

49756567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32049227-A-G

49756609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049196-G-A

49756609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049196-G-C

49756609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049196-G-T

49756613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049193-A-T

http://identifiers.org/hco/10/GRCh38#49756629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32049177-C-A

49756629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049177-C-T

49756651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049171-G-A

49756651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049171-G-T

49756684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049164-T-A

49756684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049164-T-C

49756684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049164-T-G

49756700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049148-A-G

http://identifiers.org/hco/10/GRCh38#49756722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32049133-C-A

49756722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049133-C-G

49756722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049133-C-T

http://identifiers.org/hco/10/GRCh38#49756723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32049132-C-A

49756723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049132-C-T

http://identifiers.org/hco/10/GRCh38#49756724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32049131-A-C

49756724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049131-A-G

49756861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32049019-C-T

49756885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32048995-C-T

http://identifiers.org/hco/10/GRCh38#49756974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32048906-C-A

http://identifiers.org/hco/10/GRCh38#49757020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32048878-C-A

49757043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048858-G-A

49757043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048858-G-T

http://identifiers.org/hco/10/GRCh38#49757051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32048850-C-A

http://identifiers.org/hco/10/GRCh38#49757054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32048847-C-A

49757054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048847-C-T

49757513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048720-A-G

49757521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048712-C-T

49757773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048465-T-C

49757821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048420-T-C

49757922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048350-G-C

49757931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048341-T-C

49757947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048325-G-A

49758042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048282-T-G

49758149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048183-G-A

49758224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048110-G-A

49758251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048059-A-G

http://identifiers.org/hco/10/GRCh38#49758281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32048047-C-A

49758281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048047-C-T

49758284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048044-G-T

49758334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048003-G-A

49758334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048003-G-T

49758356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047978-T-C

49758474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32047868-A-G

49758563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32047779-A-G

49758650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047684-T-G

49758676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047659-G-A

49758676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047659-G-T

49758683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047652-T-C

49758718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047619-G-A

49758718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047619-G-T

http://identifiers.org/hco/10/GRCh38#49758754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32047586-C-A

49758807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047532-A-G

49758822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047519-G-T

49758834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047507-C-T

49758930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047465-C-T

http://identifiers.org/hco/10/GRCh38#49759172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32046836-C-A

49759172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046836-C-T

49759227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046781-A-G

49759272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046738-T-C

49759288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046722-G-T

49760086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045896-C-G

49760096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045886-G-A

49760229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045759-C-T

http://identifiers.org/hco/10/GRCh38#49760292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32045726-A-C

49760334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045686-G-A

49760616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045579-C-T

49760788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045514-T-C

49760802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045500-C-T

http://identifiers.org/hco/10/GRCh38#49760859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32045470-A-C

49761059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045284-C-T

49761173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045152-G-T

49761224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045128-A-G

http://identifiers.org/hco/10/GRCh38#49761510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32044889-A-C

49761559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044777-G-A

49761575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044764-T-C

http://identifiers.org/hco/10/GRCh38#49761715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32044601-A-C

49761772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044553-A-G

49761859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32044464-T-C

http://identifiers.org/hco/10/GRCh38#49761880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32044444-A-C

49761919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044379-G-A

49761968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 32044319-C-T

49762003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044284-C-G

49762017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32044272-C-G

49762017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32044272-C-T

49762226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32044084-C-T

49762313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32044001-G-A

49762313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32044001-G-T