116100856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: 34294545-G-A

116100856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: 34294545-G-C

116100856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: 34294545-G-T

http://identifiers.org/hco/6/GRCh38#116100868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34294536-C-A

116100868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: 34294536-C-G

116100868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: 34294536-C-T

116100886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294495-G-A

116100886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294495-G-T

http://identifiers.org/hco/6/GRCh38#116100887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#34294494-C-A

116100887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294494-C-T

116100888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294493-A-G

116100888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294493-A-T

116100912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5 prime UTR variant
orthologous variants: 34294469-T-C

http://identifiers.org/hco/6/GRCh38#116100917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#34294464-C-A

116100917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294464-C-G

116100917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34294464-C-T

116100951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: synonymous_variant, undefined
orthologous variants: 34294427-G-A

116100951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: synonymous_variant, undefined
orthologous variants: 34294427-G-T

116100952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: 34294426-G-A

116100952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: 34294426-G-T

116100964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: 34294414-G-A

116100964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: 34294414-G-T

116100973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: 34294405-T-G

http://identifiers.org/hco/6/GRCh38#116101006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#34294372-C-A

116101006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, undefined
orthologous variants: 34294372-C-G

116101006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: synonymous_variant, undefined
orthologous variants: 34294372-C-T

116101075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, undefined
orthologous variants: 34294321-G-A

116101075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, undefined
orthologous variants: 34294321-G-T

116101125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294303-T-A

116101125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294303-T-C

116101125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294303-T-G

116101310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294210-T-A

116101324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294196-G-A

116101324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294196-G-T

116101336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294184-G-A

116101336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294184-G-C

116101350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294172-G-C

116101477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34294050-G-T

116101720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34293832-A-G

116102575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34293193-C-T

116102716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34293061-G-A

116102826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34292950-A-G

116102937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34292840-C-G

http://identifiers.org/hco/6/GRCh38#116102947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34292830-C-A

116104659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34289164-G-A

116104772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34289051-C-G

116104773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34289050-G-A

http://identifiers.org/hco/6/GRCh38#116104972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34288707-A-C

116104972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34288707-A-G

116105067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34288637-A-G

116105078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34288626-T-C

116105195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34288519-C-T

116106110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287583-G-A

116106110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287583-G-C

116106110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287583-G-T

116106120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287575-A-G

http://identifiers.org/hco/6/GRCh38#116106141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34287557-C-A

116106141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287557-C-G

116106141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287557-C-T

http://identifiers.org/hco/6/GRCh38#116106149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34287549-C-A

116106251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: 34287446-A-G

116106277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: 34287420-A-G

116106286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: 34287411-G-A

116106321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: synonymous variant
orthologous variants: 34287376-G-A

116106321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: 34287376-G-T

116106341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287356-T-C

116106341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287356-T-G

116106352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287345-T-C

116106357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287340-T-C

116106357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287340-T-G

116106370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287336-T-A

116106370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287336-T-C

http://identifiers.org/hco/6/GRCh38#116106372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34287334-C-A

116106372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287334-C-T

116106388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287317-A-G

116106388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287317-A-T

116106392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287313-G-A

116106392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287313-G-T

http://identifiers.org/hco/6/GRCh38#116106402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34287303-A-C

116106402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287303-A-G

116106402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287303-A-T

116106429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287276-G-T

116106475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287231-A-G

116106475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287231-A-T

116106561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34287151-A-G

http://identifiers.org/hco/6/GRCh38#116106584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34287130-A-C

116106654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34286319-T-A

116106662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34286312-A-G

116107230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, undefined
orthologous variants: 34284466-G-A

116107238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, undefined
orthologous variants: 34284458-A-G

116107411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34284292-G-A

116107892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34284250-G-A

116107892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34284250-G-C

116107933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34284208-G-A

116108012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34284118-G-A

http://identifiers.org/hco/6/GRCh38#116108056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34283849-C-A

116108329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283635-A-G

116108329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283635-A-T

116108330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283634-G-A

116108330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283634-G-T

116108351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283613-T-C

116108395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: 34283569-G-A

http://identifiers.org/hco/6/GRCh38#116108445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34283519-C-A

116108450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283514-T-A

116108450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283514-T-C

116108503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283475-T-A

http://identifiers.org/hco/6/GRCh38#116108506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34283472-C-A

116108506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283472-C-T

116108519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283454-G-T

116108547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283432-G-C

116108547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283432-G-T

http://identifiers.org/hco/6/GRCh38#116108552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34283427-C-A

116108552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283427-C-T

116108650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283403-A-G

116108699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283358-A-G

116108699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34283358-A-T

116108729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281822-G-C

116108836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281716-C-G

116108843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281709-C-T

116108967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281648-A-G

116109032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281599-A-G

116109057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281574-C-T

116109079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281552-T-C

116109125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281506-A-G

116109173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281459-A-G

116109215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281420-C-T

http://identifiers.org/hco/6/GRCh38#116109229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34281406-C-A

http://identifiers.org/hco/6/GRCh38#116109543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34281130-C-A

116109670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34281016-C-T

116110540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34280279-G-A

116110605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34280200-G-C

116110651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34280153-G-T

http://identifiers.org/hco/6/GRCh38#116110675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34280049-C-A

116110675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34280049-C-G

116110675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34280049-C-T

116110737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279940-A-G

116110772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279855-G-T

116110774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279853-T-C

116110786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279841-A-G

116110786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279841-A-T

116110800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279827-G-A

116110800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34279827-G-C

http://identifiers.org/hco/6/GRCh38#116110930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#34279701-C-A

116110930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34279701-C-G

116110930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34279701-C-T

116110960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279641-T-A

116110990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279624-T-C

116111072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279538-G-A

116111072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279538-G-T

116111086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279524-T-A

116111099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279511-A-G

116111233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34279356-C-T

116111897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278788-A-T

116111985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34278641-C-T

116112115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278509-G-C

116114924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34277034-A-T

http://identifiers.org/hco/6/GRCh38#116114928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34277030-A-C

116114976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276986-C-G

116115189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276779-A-T

116115226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34276741-A-G

http://identifiers.org/hco/6/GRCh38#116115288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34276677-C-A

116115600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275896-A-T

http://identifiers.org/hco/6/GRCh38#116115612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#34275883-C-A

116115612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275883-C-T

http://identifiers.org/hco/6/GRCh38#116115620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34275875-C-A

116115620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275875-C-T

116115702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34275800-T-C

116115779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275723-G-A

116115779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275723-G-C

116115779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275723-G-T

116115794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275667-A-G

116115802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275659-T-C

116115830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275628-T-A

116115830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275628-T-C

http://identifiers.org/hco/6/GRCh38#116115889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34275569-C-A

116115889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275569-C-T

116115920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275538-G-C

116115920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275538-G-T

http://identifiers.org/hco/6/GRCh38#116115924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34275533-A-C

116116031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275424-C-T

116116127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275338-T-C

116116201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34275291-T-G

http://identifiers.org/hco/6/GRCh38#116116879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34274778-A-C

116116879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274778-A-T

116116934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274725-C-G

116117810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274245-T-A

116117810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274245-T-C

116117810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34274245-T-G

116117993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34274061-G-A

http://identifiers.org/hco/6/GRCh38#116118187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34273871-C-A

116118187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34273871-C-T

116118229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34273837-T-G

116118473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34273609-T-C

116118496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34273587-C-G

116118713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34273359-C-G

116118804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34273263-G-T

116119623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34272493-A-G

116119690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34272430-A-G

116119872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34272269-A-G

116119886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34272255-T-C

116120110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34272033-T-C

http://identifiers.org/hco/6/GRCh38#116120191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34271952-A-C

116120482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34271661-C-T

116121241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270902-G-A

http://identifiers.org/hco/6/GRCh38#116121386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#34270757-C-A

116121386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270757-C-T

116121514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270629-T-C

116121578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270565-C-G

116121581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270562-G-A

116121581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270562-G-C

http://identifiers.org/hco/6/GRCh38#116121761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#34270382-C-A

116121761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34270382-C-T

116121980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270164-A-G

116121991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270154-T-C

116122003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270152-G-C

116122009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270146-G-T

http://identifiers.org/hco/6/GRCh38#116122065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34270099-A-C

116122065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270099-A-G

116122094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270061-T-C

116122441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34270006-G-A

http://identifiers.org/hco/6/GRCh38#116123137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34268790-A-C

116123138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34268789-G-A

116123332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34268596-G-C

116123753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34268153-G-A

116123893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34268002-T-C

116124363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267584-G-A

116124363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267584-G-C

116124381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267567-T-C

116124400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267548-G-T

116124492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267455-G-A

116124503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267444-A-G

116124520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267428-A-G

116124733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267288-A-G

116124809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34267217-T-C

116125129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266970-C-G

116125203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266910-T-C

116125203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266910-T-G

116125229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266879-G-T

http://identifiers.org/hco/6/GRCh38#116125259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34266852-C-A

116125259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266852-C-T

116125482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34266626-T-C

116125513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 34266595-A-G

116125525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34266583-A-G

116125579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34266530-A-G

116125825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34266257-T-G

116125963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266128-C-G

116125963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34266128-C-T

http://identifiers.org/hco/6/GRCh38#116126137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34265969-C-A

116126213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34265891-T-C

116126259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34265845-G-A

116126427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34265685-A-G

116126513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34265610-T-C

116126593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34265477-A-G

http://identifiers.org/hco/6/GRCh38#116126661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34265296-C-A

116126661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34265296-C-G

116127153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34264809-C-T

116127224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34264745-G-C

116127303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34264663-T-C

116127469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34262603-A-G

116127587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34262476-G-A

116128089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34262042-A-T

116128123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34262003-G-A

116128264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261871-C-T

116128400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261734-T-C

116128547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261591-A-T

116128631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261523-A-G

116128806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261376-G-A

116128809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261373-A-G

116129073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261116-A-G

116130228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34261048-C-T

http://identifiers.org/hco/6/GRCh38#116130316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34260949-A-C

116130367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34260919-A-G

116130402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34260885-C-T

116131945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34259477-A-G

116132787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34258635-T-C

116132991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34258414-T-C

116133466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34258002-A-G

116133518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34257969-A-G

116133930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34257382-T-C

116133937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34257375-C-T

116133995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34257322-A-G

116133995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34257322-A-T

116134439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34256976-A-G

116135208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34256052-A-G

116135215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34256045-A-T

116143920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34253355-T-G

116144115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34253129-C-T

116144192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34253064-T-C

116144616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34252900-A-G

116144771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34252791-G-A

116144782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34252780-A-G

116144883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34252699-G-A

116144904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34252684-G-A

116145058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34252526-A-T

http://identifiers.org/hco/6/GRCh38#116145406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34250668-C-A

116145406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34250668-C-T

116145487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34250600-A-G

116145487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 34250600-A-T

116148208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34250507-G-T

116148427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34250295-G-T

116148499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34250226-T-C

116148908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34249664-A-G

116149217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34249355-T-C

http://identifiers.org/hco/6/GRCh38#116149409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34249198-C-A

116149518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34249090-C-G

116149594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34249007-A-G

116149619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34248984-A-G

116149633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34248971-A-G

116149741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34248867-G-A

116149863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34248767-T-G

116150089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34248544-T-C

http://identifiers.org/hco/6/GRCh38#116151215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34247763-C-A

116151314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34247675-G-C

116151549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34247219-G-A

116151573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34247192-G-A

116151715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34247045-G-C

116151886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34246857-T-C

116152888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34244439-G-C

116153160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34244175-A-G

116153279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34244057-A-T

116153312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243687-A-G

116153318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243683-C-T

116153374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243631-C-T

116153922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243227-G-T

116153954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243196-T-C

116153984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243114-A-G

116154130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34243006-T-C

116154291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34242498-T-G

116154525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34242278-G-A

116154747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34242096-A-G

116155033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241819-G-A

116155033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241819-G-T

116155048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241798-A-G

116155290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241439-A-G

http://identifiers.org/hco/6/GRCh38#116155330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34241401-C-A

116155338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241393-T-C

116155456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241309-C-G

116155579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241173-T-A

116155711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241051-A-T

116155719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241044-T-A

116155719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241044-T-C

http://identifiers.org/hco/6/GRCh38#116155724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34241039-C-A

http://identifiers.org/hco/6/GRCh38#116155729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34241034-C-A

116155743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34241020-A-G

116155784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240990-T-C

116155817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240957-G-T

116155833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240941-G-C

116155927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240847-G-A

116156040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240750-T-C

116156345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240475-A-G

116156502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240300-A-T

116156676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 34240145-A-G

116156781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34240045-G-A

http://identifiers.org/hco/6/GRCh38#116156832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34239996-C-A

116156870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 34239960-C-G

116157373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34239454-G-A

116157373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34239454-G-T

116157485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34239339-C-G

116157718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34239118-A-T

116157769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34239050-C-G

116157907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34238931-G-T

116158358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34236408-T-C

116171248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34234299-A-G

http://identifiers.org/hco/6/GRCh38#116171415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34234141-A-C

116171502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34234051-G-C

116171649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34233720-C-T

116171695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34233663-G-A

116175935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232779-G-A

116175950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232764-G-A

116176006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232718-C-T

116176074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232644-C-T

116176113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232606-C-T

116176366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232363-G-C

116176626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232159-C-T

116176635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34232150-A-G

116176832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34231886-C-G

116177005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34229083-G-T

116177052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34229055-G-A

116177242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34228488-T-C

116177355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34228397-G-A

116177453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34228299-A-G

116177486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34228267-G-T

116189184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34225042-G-A

116189558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34224702-T-C

116197324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34223231-A-G

116197924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34219479-C-T

116198410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218961-G-T

116198901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218788-A-T

116199090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218557-C-T

116199132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218507-C-T

116199149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218484-C-T

116201851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218227-A-G

116202034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34218047-G-T

116202207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34217865-A-G

http://identifiers.org/hco/6/GRCh38#116202310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34217754-A-C

http://identifiers.org/hco/6/GRCh38#116202312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34217752-C-A

116202582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34217381-C-T

116203309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34216501-T-C

116203402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34216434-T-C

116207939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34215657-C-T

116208200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34215411-C-T

116215916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34206221-T-C

http://identifiers.org/hco/6/GRCh38#116215939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34206193-C-A

116216587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204988-A-G

116216587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204988-A-T

116216605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204970-A-G

116216889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204725-C-T

116217207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204440-T-C

116217240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 34204411-A-T

116217262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204384-T-C

116217306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204340-A-G

116217306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204340-A-T

116217307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204339-G-A

116217355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204293-C-T

116217570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204080-T-C

116217601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34204023-G-A

116217715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34203907-C-T

116217814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34203770-T-C

116218018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34203158-T-C

116218222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34202989-A-G

116218404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34202819-C-T

116218590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34202693-T-C

http://identifiers.org/hco/6/GRCh38#116218856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34202404-A-C

116219387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34202117-T-G

116220168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34201531-T-A

http://identifiers.org/hco/6/GRCh38#116220190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34201509-C-A

116220190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34201509-C-T

116220607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34201246-G-A

116220618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34201235-C-G

http://identifiers.org/hco/6/GRCh38#116220922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34200604-C-A

116220997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34200509-A-G

116221037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34200473-A-G

116221037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34200473-A-T

116221065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 34200445-A-G

116221085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 34200425-A-T

116221101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 34200409-T-C

116221252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34200258-T-A

116222059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34199729-C-T

116222348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34199460-T-C

116222769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34199088-G-C

116222804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198925-C-T

116222889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198831-G-A

116222889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198831-G-C

116222938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198779-G-A

116222938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198779-G-T

116223000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198725-A-T

http://identifiers.org/hco/6/GRCh38#116223008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34198717-C-A

116223008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198717-C-G

116223125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 34198609-A-G

116223125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 34198609-A-T

116223169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198554-G-C

116223172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198551-G-T

http://identifiers.org/hco/6/GRCh38#116223228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34198504-C-A

116223228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198504-C-G

116223228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198504-C-T

http://identifiers.org/hco/6/GRCh38#116223256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34198478-C-A

116223256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34198478-C-T

116227909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194342-T-C

116227915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194336-C-T

116227926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194325-C-T

116227933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194318-C-G

116227933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194318-C-T

116227937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194314-G-A

116227937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194314-G-C

116227948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194299-G-A

116228186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34194113-A-G

116228960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34193697-T-G

116228990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34193683-T-C

116229075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34193608-T-G

116229286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34193408-C-T

116229434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34193174-A-G

http://identifiers.org/hco/6/GRCh38#116229476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34193132-A-C

116229476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34193132-A-T

116229693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34192940-C-T

116230450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34192324-T-C

116230747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34192008-T-G

116230903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34191874-A-T

116236819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190961-T-C

116236819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190961-T-G

116236885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190910-A-T

116236894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190906-C-G

http://identifiers.org/hco/6/GRCh38#116236909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34190895-C-A

116236971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 34190857-G-A

116236974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 34190854-G-A

http://identifiers.org/hco/6/GRCh38#116237007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34190821-C-A

116237123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190701-G-A

116237123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190701-G-T

116237137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190654-T-A

116237137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190654-T-C

116237149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190628-A-G

116237175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190603-T-A

116237209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190579-T-C

116237369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190420-G-T

116237377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190412-A-G

116237377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34190412-A-T

http://identifiers.org/hco/6/GRCh38#116237393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34190396-C-A

116237494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34190322-C-G

116237494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34190322-C-T

116237571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34190250-G-T

116237640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 34190180-G-A

116237703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34190128-G-C

116237708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34190123-A-G

116237709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34190122-A-G

116237885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34189985-A-G

116237896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34189974-C-T

116238127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34189790-G-A

116238127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 34189790-G-T

116238152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189767-T-C

116238363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189569-C-T

116238375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189557-T-C

116238384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189549-A-G

116238407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189516-G-C

116238407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189516-G-T

http://identifiers.org/hco/6/GRCh38#116238411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34189512-C-A

116238411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189512-C-G

116238411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34189512-C-T

116238493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186901-T-A

116238493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186901-T-G

116238822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186598-T-C

116238849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186571-A-G

116238849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186571-A-T

116238859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186561-A-G

116238896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 34186525-A-G

http://identifiers.org/hco/6/GRCh38#116238960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34186458-A-C

116238977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 34186441-A-G

116239045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 34186373-T-C

116239046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 34186372-C-G

116239046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 34186372-C-T

116239144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34186275-A-G

116239205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34186217-G-T

http://identifiers.org/hco/6/GRCh38#116239220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34186202-C-A

116239220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34186202-C-T

http://identifiers.org/hco/6/GRCh38#116239248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34185970-C-A

116239268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34185911-A-G

116239369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34185818-G-A

116239369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34185818-G-T

116239624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34185661-T-A

116243871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34181016-A-G

116243886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34181001-T-A

116243893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34180994-T-A

116243895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34180992-T-C

116243895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron variant
orthologous variants: 34180992-T-G

116243902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34180985-T-C

http://identifiers.org/hco/6/GRCh38#116243903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34180979-C-A

116243903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 34180979-C-T

116243946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: synonymous variant
orthologous variants: 34180936-A-G

http://identifiers.org/hco/6/GRCh38#116243957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34180925-A-C

116243982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: synonymous variant
orthologous variants: 34180898-T-C

116244015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: missense variant
orthologous variants: 34180869-A-G

116244044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180844-G-C

116244044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180844-G-T

116244045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180843-A-G

116244251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180606-T-A

116244270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180592-C-T

http://identifiers.org/hco/6/GRCh38#116244280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34180582-C-A

116244280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180582-C-G

116244332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180545-T-A

116244332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180545-T-C

116244332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180545-T-G

116244339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180538-G-A

116244339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180538-G-C

116244339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34180538-G-T

http://identifiers.org/hco/6/GRCh38#116244363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#34180515-C-A

116244412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34180469-T-C

116244439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34180442-G-T

116244461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34180420-G-T

116244466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34180417-T-C

116244468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34180415-A-G

116244474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34180409-T-G

116244490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 34180392-A-G

116244983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180217-T-G

116245159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180084-A-G

116245170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180071-A-G

116245208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34180028-A-G

116245443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21556
most severe consequence: 3 prime UTR variant
orthologous variants: 34179836-G-T