69298932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5 prime UTR variant
orthologous variants: 61934099-G-A

69298932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5 prime UTR variant
orthologous variants: 61934099-G-T

69299165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933885-A-G

69299179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933872-C-T

69299213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933840-G-C

69299415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933692-G-C

69299507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933575-C-G

69299632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933344-C-T

http://identifiers.org/hco/15/GRCh38#69299742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#61933220-C-A

69299832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933137-G-T

69299976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61933010-G-A

http://identifiers.org/hco/15/GRCh38#69301423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61932266-C-A

http://identifiers.org/hco/15/GRCh38#69301630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61932097-A-C

69301675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61932030-T-G

69301680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61932025-G-A

69301725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931967-T-C

69301850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931818-T-C

69301850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931818-T-G

69303713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931587-C-G

http://identifiers.org/hco/15/GRCh38#69303905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61931395-C-A

69304133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931187-A-G

69304209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931140-G-T

69304239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931111-T-G

69304339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61931022-T-G

69304540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61930856-A-T

69304582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61930817-A-G

69304582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61930817-A-T

69304652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61930748-A-G

69304804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61930569-G-A

69305053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61930310-A-T

69305513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61929319-T-G

69305990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61928981-A-G

69306174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61928841-C-T

69306188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61928821-G-A

69306188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61928821-G-T

69306780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61928272-A-G

69306787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61928267-T-A

69307406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61927183-G-A

69307411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61927178-T-G

http://identifiers.org/hco/15/GRCh38#69307931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61926744-C-A

69307931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926744-C-T

http://identifiers.org/hco/15/GRCh38#69307985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61926692-C-A

69307985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926692-C-T

69307999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926675-C-G

69307999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926675-C-T

69308008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926666-G-A

69308176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926190-C-T

http://identifiers.org/hco/15/GRCh38#69308243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61926122-C-A

69308243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926122-C-G

69308243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61926122-C-T

69308904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61924970-G-A

69308970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61924903-A-G

69309026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61924848-G-A

69311379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61922712-C-T

69311457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61922633-A-G

69312003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61922011-C-G

69312003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61922011-C-T

69312342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61921325-G-A

69312342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61921325-G-C

69312342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61921325-G-T

http://identifiers.org/hco/15/GRCh38#69313660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61920762-C-A

69313661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61920761-C-T

http://identifiers.org/hco/15/GRCh38#69313787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61920660-A-C

69313835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61920624-C-T

69314329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61920180-G-A

69314330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61920179-G-T

69314351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61920157-G-T

http://identifiers.org/hco/15/GRCh38#69314415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61920106-C-A

69314501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61920023-T-C

http://identifiers.org/hco/15/GRCh38#69314546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61919989-C-A

69314572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61919969-T-C

69314596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61919945-A-T

69314601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61919940-T-C

http://identifiers.org/hco/15/GRCh38#69314648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61919910-C-A

69314648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61919910-C-G

69314648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61919910-C-T

69314713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61919859-G-T

69314914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61919639-T-A

69314914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61919639-T-C

69315556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61918478-C-G

http://identifiers.org/hco/15/GRCh38#69315655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61918374-A-C

69315655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61918374-A-G

69315668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61918355-C-T

69315831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61918184-G-A

69316037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61918009-G-C

69316095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61917950-T-C

69316343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61917662-G-A

69316343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61917662-G-T

69316376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61917611-C-G

69316376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61917611-C-T

69317478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61915950-C-G

69317478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61915950-C-T

69317787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61915634-C-T

69318038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61915408-C-T

69318124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61915320-C-T

69318220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61915236-A-G

69320257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61914268-G-A

69320277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61914255-C-G

69320360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61914155-A-G

http://identifiers.org/hco/15/GRCh38#69320569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61914012-A-C

69320806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61913609-C-T

69322698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912563-G-T

http://identifiers.org/hco/15/GRCh38#69322745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61912507-A-C

69322745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912507-A-G

69322750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912502-A-G

69322756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912496-A-G

69322756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912496-A-T

69322765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912487-A-G

69322765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912487-A-T

69322775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912477-A-G

69322781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912471-A-G

69322811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61912441-G-A

69323235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911990-A-G

69323250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911976-C-G

69323288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911944-C-T

69323470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911769-C-T

69323772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911495-C-T

69323861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911389-T-G

69323935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911318-T-A

69324247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911049-C-T

69324266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911030-G-A

69324269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911022-T-C

69324269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61911022-T-G

http://identifiers.org/hco/15/GRCh38#69324328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61910967-C-A

69324328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61910967-C-T

69324514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61910754-A-G

69324537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61910699-T-A

69324638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61910592-T-C

69325927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61909444-G-A

http://identifiers.org/hco/15/GRCh38#69326013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61909365-C-A

69326021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61909357-T-C

69328168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906688-G-A

69328243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906622-A-G

69328359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906519-G-A

69328379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906499-G-A

69328380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906498-A-T

69328440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906459-C-T

69328564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906348-G-A

69328602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906306-C-T

http://identifiers.org/hco/15/GRCh38#69328689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61906229-A-C

69328732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61906184-T-C

69328748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906175-A-G

69328751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61906172-C-T

69328787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61906142-T-A

69328992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61905925-G-C

69328994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61905923-A-G

http://identifiers.org/hco/15/GRCh38#69329026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#61905899-C-A

69329026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61905899-C-T

69329045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61905880-A-T

69329116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61905817-G-A

69358178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61898196-G-A

69358202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61898172-T-A

69358656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61897754-G-A

69358656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61897754-G-T

69358722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61897673-C-T

69358723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61897672-C-T

http://identifiers.org/hco/15/GRCh38#69358793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61897604-C-A

69358793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61897604-C-T

69359075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61897370-G-C

69359176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61897268-G-A

69359256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61897191-C-T

69359840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61896543-A-G

69359840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61896543-A-T

http://identifiers.org/hco/15/GRCh38#69359858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61896516-C-A

69359858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61896516-C-G

69359858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61896516-C-T

69359886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61896494-T-C

69359889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61896491-T-C

69360152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896256-G-C

http://identifiers.org/hco/15/GRCh38#69360181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61896228-C-A

69360181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896228-C-T

69360201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896208-G-T

69360204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896201-G-A

http://identifiers.org/hco/15/GRCh38#69360212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61896193-C-A

69360212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896193-C-T

69360237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896183-A-G

69360237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896183-A-T

69360248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896172-G-A

69360248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896172-G-T

69360297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896130-C-T

69360538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895786-G-T

69360562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895762-C-T

69360579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895743-G-C

69360668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895683-C-T

69360827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895532-G-A

69361340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895065-G-A

69375025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890147-T-G

http://identifiers.org/hco/15/GRCh38#69375147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61890027-C-A

69375147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890027-C-T

69375710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889422-C-G

69375755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889381-C-T

69375817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889316-G-A

69376053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889094-G-A

69376359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888791-A-G

69376401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888749-A-T

69376496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888655-A-G

69376555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888595-A-G

69376602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888543-C-T

69376878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888019-C-T

69377323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887189-C-T

69377325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887187-A-G

69379279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884049-T-G

69379282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884046-T-G

69379314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884005-G-A

69379789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61883560-A-G

69379794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61883555-C-T

http://identifiers.org/hco/15/GRCh38#69380062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61883302-C-A

http://identifiers.org/hco/15/GRCh38#69380197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61883191-C-A

69380201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61883187-T-A

http://identifiers.org/hco/15/GRCh38#69380239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61883169-A-C

69380239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61883169-A-G

69380323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61883102-A-G

69380328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61883097-T-C

69380348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61883077-A-G

69380696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61882548-G-A

69381595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880780-C-T

69381954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880462-G-A

69381955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880461-G-A

69381968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880447-G-A

http://identifiers.org/hco/15/GRCh38#69382982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61880379-C-A

69382982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880379-C-T

http://identifiers.org/hco/15/GRCh38#69383068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61880286-C-A

69383068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880286-C-T

69383073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880281-G-A

http://identifiers.org/hco/15/GRCh38#69383115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61880240-C-A

69383115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880240-C-T

69383174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880167-G-A

69384783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61880005-C-G

69384783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61880005-C-T

http://identifiers.org/hco/15/GRCh38#69384909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61879879-C-A

69384909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879879-C-T

69384910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879878-T-C

69384929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879864-T-C

http://identifiers.org/hco/15/GRCh38#69384936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61879859-C-A

69384985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879826-G-A

69384985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879826-G-T

69385400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879473-T-C

69385451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879428-T-A

69385615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879259-A-G

69385644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879226-G-C

69385770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879077-A-G

http://identifiers.org/hco/15/GRCh38#69389070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61876701-C-A

69389070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876701-C-G

69389078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876693-T-C

69389337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876493-C-G

69389409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876420-G-A

69389428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876386-G-A

69390540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61875120-G-A

http://identifiers.org/hco/15/GRCh38#69390694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61874970-C-A

69390780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874864-C-T

69390810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874812-A-G

69390878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874750-G-A

69390929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874699-T-C

69391054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874599-G-A

69391054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874599-G-T

69391063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874590-A-T

69391064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61874589-G-A

http://identifiers.org/hco/15/GRCh38#69391170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61874526-A-C

69391386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61874369-T-A

http://identifiers.org/hco/15/GRCh38#69391387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61874368-C-A

69391387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61874368-C-T

http://identifiers.org/hco/15/GRCh38#69391393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61874362-C-A

69391393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61874362-C-T

69391405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61874347-G-A

69391704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61873858-A-G

69391720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 61873842-G-C

69391720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 61873842-G-T

http://identifiers.org/hco/15/GRCh38#69391742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61873830-C-A

69392323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61873631-A-G

69392624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61873356-A-T

69394885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 61872997-T-C

69395046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61872846-C-G

69395166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61872740-G-T

69395668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, undefined
orthologous variants: 61872412-C-T

69396692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61871784-G-A

69396692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61871784-G-C

69396780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61871716-C-T

69396807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61871688-T-C

69396873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61871625-G-A

69396873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron variant
orthologous variants: 61871625-G-T

69396919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871580-T-C

69397022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871478-A-G

69397041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871455-A-T

http://identifiers.org/hco/15/GRCh38#69397053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61871443-C-A

69397053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871443-C-T

http://identifiers.org/hco/15/GRCh38#69397074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61871422-C-A

69397074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871422-C-T

69397201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871341-C-T

69397230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871317-G-A

69397230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871317-G-T

69397238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871309-T-C

69397238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871309-T-G

69397303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871252-G-A

http://identifiers.org/hco/15/GRCh38#69397339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61871217-C-A

69397363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871173-T-C

69397391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61871153-T-C

69397462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 61871110-A-G

69397478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61871094-A-G

69397478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61871094-A-T

http://identifiers.org/hco/15/GRCh38#69397592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61870976-C-A

http://identifiers.org/hco/15/GRCh38#69397654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61870918-A-C

69397654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61870918-A-G

69397679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61870909-G-T

69397750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 61870891-T-A

69397872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870884-T-C

69397912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870861-A-G

69397912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870861-A-T

69397919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870854-A-G

69397919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870854-A-T

69398248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870644-G-C

69398252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870640-T-A

69398328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870568-C-T

69398463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870438-A-G

69398498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870401-A-G

69399851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61869018-G-A

69399851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61869018-G-T

69400052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61868872-G-C

69400061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 61868863-T-C

69400086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61868838-G-A

69400164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868789-G-A

http://identifiers.org/hco/15/GRCh38#69400176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61868774-C-A

69400176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868774-C-T

69400215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868732-G-T

69400251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868661-T-C

69400559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868409-G-A

http://identifiers.org/hco/15/GRCh38#69401171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61867794-C-A

69401171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61867794-C-T

69403547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863601-T-C

69403717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 61863431-T-C

69403923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61863258-T-A

69404568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862480-T-A

69404568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862480-T-C

69404568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862480-T-G

69404593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862456-A-G

69404672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862379-G-T

69404695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862356-G-T

69404718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862334-T-C

69404867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862189-G-T

69405051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862038-T-C

69405147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861022-G-A

69405147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861022-G-T

69405421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61860704-G-T

http://identifiers.org/hco/15/GRCh38#69405438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#61860687-C-A

69405554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61860568-G-A