http://identifiers.org/hco/2/GRCh38#238100345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91249777-C-A

238100345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5 prime UTR variant
orthologous variants: 91249777-C-T

http://identifiers.org/hco/2/GRCh38#238100494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91249929-C-A

238100494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91249929-C-G

238100494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91249929-C-T

238100527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91249962-G-A

238100527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91249962-G-T

http://identifiers.org/hco/2/GRCh38#238100575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91250010-C-A

238100575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250010-C-T

http://identifiers.org/hco/2/GRCh38#238100605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91250040-C-A

238100605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250040-C-T

238100653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250088-T-C

http://identifiers.org/hco/2/GRCh38#238100690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91250125-C-A

238100690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: 91250125-C-T

238100698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250133-G-A

238100698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250133-G-T

http://identifiers.org/hco/2/GRCh38#238100701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91250136-C-A

238100701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250136-C-T

238100710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250145-G-A

238100710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250145-G-C

238100710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91250145-G-T

238100731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250166-A-G

238100731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250166-A-T

238100790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250208-A-G

238100816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250220-G-T

238101069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250501-C-T

238101070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250502-T-C

238101200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250639-C-T

238101227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91250662-C-T

238101683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251036-C-T

238101740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251080-C-T

http://identifiers.org/hco/2/GRCh38#238101916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91251176-C-A

238101916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251176-C-T

http://identifiers.org/hco/2/GRCh38#238101964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91251224-C-A

http://identifiers.org/hco/2/GRCh38#238102001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91251261-C-A

238102001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91251261-C-T

238102030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91251290-C-T

http://identifiers.org/hco/2/GRCh38#238102119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91251379-C-A

238102119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: 91251379-C-T

http://identifiers.org/hco/2/GRCh38#238102176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91251421-C-A

238102176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251421-C-T

238102189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251439-G-T

238102238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251493-A-G

238103922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251891-T-G

http://identifiers.org/hco/2/GRCh38#238103940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91251904-C-A

238103940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91251904-C-G

238104072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91252038-C-T

http://identifiers.org/hco/2/GRCh38#238104371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91252378-A-C

http://identifiers.org/hco/2/GRCh38#238104526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91252512-C-A

238104526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91252512-C-G

238104598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91252584-G-A

238104598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91252584-G-T

238104670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: 91252772-G-A

238104670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: 91252772-G-T

http://identifiers.org/hco/2/GRCh38#238104683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91252785-C-A

238104683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91252785-C-T

http://identifiers.org/hco/2/GRCh38#238104761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91252863-C-A

238104761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: 91252863-C-G

238104761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91252863-C-T

238104815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91252917-T-A

238104815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91252917-T-C

http://identifiers.org/hco/2/GRCh38#238104948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91253038-C-A

238104948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253038-C-T

238105222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253230-C-T

238105236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253244-A-G

238105534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253543-A-G

238105534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253543-A-T

238105684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253695-G-A

238105867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253829-G-A

238105867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253829-G-T

238105880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253840-T-C

238105977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253904-G-A

238106092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253948-C-G

238106092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253948-C-T

238106165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91253997-C-T

238106497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91254270-C-G

238106513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91254286-G-A

http://identifiers.org/hco/2/GRCh38#238106584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91254324-C-A

238106584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91254324-C-T

238106812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91254475-G-A

238106872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91254528-C-G

238107344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91254808-G-T

238107498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91254913-C-T

238107503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91254918-C-T

238107656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91255050-G-A

238107656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91255050-G-T

238107658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91255052-G-C

238107658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91255052-G-T

238107761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255150-T-C

238107761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255150-T-G

http://identifiers.org/hco/2/GRCh38#238107764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91255153-C-A

238107764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255153-C-G

238107764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255153-C-T

238107805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: synonymous variant
orthologous variants: 91255212-C-T

238107810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: missense variant
orthologous variants: 91255217-G-T

238108036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255434-G-T

238108089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255494-G-T

238108090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255495-G-A

238108090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91255495-G-T

238113815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91261625-C-T

238113861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91261663-G-A

238114267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262024-C-T

http://identifiers.org/hco/2/GRCh38#238114269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91262026-C-A

238114269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262026-C-T

238116804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262312-G-A

238116816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262335-G-T

238116818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262337-G-T

http://identifiers.org/hco/2/GRCh38#238116846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91262359-C-A

238116846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262359-C-T

238116899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91262408-G-A

238116914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 91262423-C-T

238116980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 91262489-G-A

238117016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 91262525-G-T

http://identifiers.org/hco/2/GRCh38#238117043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91262553-C-A

238117043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262553-C-T

http://identifiers.org/hco/2/GRCh38#238117058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91262568-C-A

238117058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262568-C-T

238117133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262621-A-G

238117134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262622-G-T

http://identifiers.org/hco/2/GRCh38#238117181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91262656-C-A

238117186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262661-G-A

238117186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262661-G-T

238117293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91262765-C-T

238119693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91263222-C-G

238119774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91263289-C-T

238120002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91263468-G-A

238120225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91263652-C-T

238120236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91263663-G-A

http://identifiers.org/hco/2/GRCh38#238120602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91264103-A-C

238120756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91264260-C-T

238121124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91264635-C-T

238121202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91264729-T-C

238121708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91264982-T-A

238122091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91265346-C-T

238122097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91265352-C-T

238122229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91265462-G-A

238122466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91265647-G-A

238122469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91265650-C-T

238122513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91265698-G-A

238123570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91266258-C-T

238123974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91266644-C-T

238124206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91266883-C-T

http://identifiers.org/hco/2/GRCh38#238124289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91266957-C-A

238125131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268103-G-A

238125131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268103-G-C

238125131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268103-G-T

http://identifiers.org/hco/2/GRCh38#238125210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268160-C-A

238125210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268160-C-T

238125287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268248-G-A

238125287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268248-G-T

http://identifiers.org/hco/2/GRCh38#238125308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268269-C-A

238125308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268269-C-G

238125308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268269-C-T

238125332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91268293-G-T

http://identifiers.org/hco/2/GRCh38#238125335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268296-C-A

238125335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268296-C-G

238125335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268296-C-T

http://identifiers.org/hco/2/GRCh38#238125365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268326-A-C

238125365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268326-A-G

238125365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91268326-A-T

238125373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91268334-G-A

238125373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91268334-G-T

http://identifiers.org/hco/2/GRCh38#238125394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268355-C-A

238125394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268355-C-G

238125394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268355-C-T

http://identifiers.org/hco/2/GRCh38#238125454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268394-C-A

238125454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268394-C-T

http://identifiers.org/hco/2/GRCh38#238125503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268442-A-C

238125503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268442-A-G

238125503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268442-A-T

238125523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268464-T-A

238125565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268490-G-T

http://identifiers.org/hco/2/GRCh38#238125628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91268544-A-C

238125792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268650-G-A

238126005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268814-C-G

238126082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268885-G-A

238126154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91268955-G-A

238126218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269001-G-A

238126222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269005-C-G

238126319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269085-A-T

238126347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269113-T-G

238126348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269114-G-C

238127220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91269153-C-T

http://identifiers.org/hco/2/GRCh38#238127303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91269219-C-A

238127325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269242-T-A

238127325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269242-T-C

238127325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269242-T-G

238127329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269246-G-C

238127329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269246-G-T

238127385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91269311-G-A

238127452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269386-A-G

238127452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269386-A-T

238127479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269425-T-C

238127479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269425-T-G

238127496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269442-G-A

238127496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269442-G-C

http://identifiers.org/hco/2/GRCh38#238127514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91269456-C-A

238127514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269456-C-T

http://identifiers.org/hco/2/GRCh38#238127543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91269488-C-A

238127545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269490-G-T

238127581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91269520-A-G

238127639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91269585-G-A

http://identifiers.org/hco/2/GRCh38#238127728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91269659-C-A

238127780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269672-A-T

238127800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269692-T-C

238127800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269692-T-G

238128069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91269891-C-T

238128382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91270075-A-G

238128490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91270126-C-T

http://identifiers.org/hco/2/GRCh38#238128650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91270207-C-A

238128650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91270207-C-G

http://identifiers.org/hco/2/GRCh38#238128672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#91270228-C-A

238128672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, undefined
orthologous variants: 91270228-C-T

238128728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 91270281-G-T

238128730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 91270283-G-A

238128730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 91270283-G-T

238128737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 91270290-T-C

238128763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 91270316-G-A

238128763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 91270316-G-C

238128763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 91270316-G-T

http://identifiers.org/hco/2/GRCh38#238128826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91270379-C-A

238128886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91270439-G-T

238128916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91270510-G-A

238128916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron variant
orthologous variants: 91270510-G-T

238128927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91270521-A-G

238128982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270718-C-T

238128992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270757-G-A

238129047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270818-C-G

238129047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270818-C-T

238129113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270872-A-G

238129216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270949-G-A

238129216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91270949-G-T

http://identifiers.org/hco/2/GRCh38#238129337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91271066-C-A

238129337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91271066-C-T

238129346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91271075-G-T

http://identifiers.org/hco/2/GRCh38#238130006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91271927-C-A

238130006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91271927-C-T

238130020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91271935-G-T

238130037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91271952-G-T

238130123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91272032-C-G

238130123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91272032-C-T

238130340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272261-C-G

238130340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272261-C-T

http://identifiers.org/hco/2/GRCh38#238130411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91272332-C-A

238130411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91272332-C-T

http://identifiers.org/hco/2/GRCh38#238130451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91272372-C-A

238130475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272396-G-A

238130550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272471-G-A

238130550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272471-G-T

http://identifiers.org/hco/2/GRCh38#238130616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91272537-C-A

238130652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272573-G-A

238130652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91272573-G-T

238130679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272600-G-A

238130679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272600-G-T

http://identifiers.org/hco/2/GRCh38#238130680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91272601-C-A

238130680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91272601-C-T

http://identifiers.org/hco/2/GRCh38#238130781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91272702-A-C

238130997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272918-G-A

238130997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91272918-G-T

238131172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273096-G-A

238131172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273096-G-T

238131256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273180-G-A

238131256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273180-G-T

238131258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273182-G-A

238131258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273182-G-T

238131276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273200-A-G

238131276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273200-A-T

238131465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273389-C-T

http://identifiers.org/hco/2/GRCh38#238131513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91273437-C-A

238131513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273437-C-G

238131513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273437-C-T

238131516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273440-C-G

238131559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273483-G-A

238131559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273483-G-C

238131559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273483-G-T

http://identifiers.org/hco/2/GRCh38#238131573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91273497-C-A

238131573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273497-C-T

238131577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273501-G-A

238131577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91273501-G-C

238131610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 91273534-C-T

http://identifiers.org/hco/2/GRCh38#238131648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91273575-C-A

238131648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91273575-C-T

238131748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273683-G-A

238131748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273683-G-T

238131770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273699-G-A

238131770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273699-G-T

238131812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273737-T-G

238131816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273741-G-T

238131829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273754-G-A

238131829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273754-G-T

http://identifiers.org/hco/2/GRCh38#238131837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91273761-C-A

238131837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273761-C-T

http://identifiers.org/hco/2/GRCh38#238131917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91273838-C-A

238131917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273838-C-G

http://identifiers.org/hco/2/GRCh38#238131927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91273848-C-A

238131945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273861-C-T

238131955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273868-G-A

238131955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91273868-G-T

238132163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274022-C-T

http://identifiers.org/hco/2/GRCh38#238132178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274043-C-A

238132178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91274043-C-T

238132259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274131-A-G

238132276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274164-G-C

238132276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274164-G-T

http://identifiers.org/hco/2/GRCh38#238132287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274175-C-A

238132287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274175-C-G

238132287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274175-C-T

http://identifiers.org/hco/2/GRCh38#238132356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274243-A-C

238132356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274243-A-G

238132361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91274248-G-T

238132397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274283-G-A

238132397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274283-G-T

http://identifiers.org/hco/2/GRCh38#238132405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274310-C-A

238132405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274310-C-T

238132482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274378-G-T

http://identifiers.org/hco/2/GRCh38#238132530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274409-C-A

238132530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274409-C-T

238132535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274414-G-A

238132535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274414-G-T

238132588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274473-G-A

http://identifiers.org/hco/2/GRCh38#238132620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274488-C-A

238132620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274488-C-T

http://identifiers.org/hco/2/GRCh38#238132665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274515-C-A

238132665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274515-C-T

238132773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274651-T-C

http://identifiers.org/hco/2/GRCh38#238132835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274714-C-A

238132835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274714-C-T

http://identifiers.org/hco/2/GRCh38#238132856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91274720-C-A

238132856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274720-C-G

238132856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274720-C-T

238132928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274780-G-T

238133032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274885-G-T

238133064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274930-A-G

238133075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274941-A-G

238133075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274941-A-T

238133076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91274942-G-A

http://identifiers.org/hco/2/GRCh38#238133143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91275004-C-A

238133143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91275004-C-T

238133246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27937
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91275129-T-G