53962700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306898-T-A

http://identifiers.org/hco/6/GRCh38#53962909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77306727-C-A

53962909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306727-C-T

53963076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306555-A-T

53963123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306518-T-A

53963123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306518-T-G

53963242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306388-G-C

http://identifiers.org/hco/6/GRCh38#53963338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77306312-C-A

53963655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305770-T-C

53963655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305770-T-G

http://identifiers.org/hco/6/GRCh38#53963915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77305500-A-C

53966236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304977-A-G

53966290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304928-A-G

53966291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304927-G-A

53966292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304926-C-G

53966433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304789-T-G

53967001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304398-G-A

53967029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304373-C-T

http://identifiers.org/hco/6/GRCh38#53967034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77304368-A-C

53967863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77302661-T-C

53968388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77302193-A-G

53968404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77302179-C-T

http://identifiers.org/hco/6/GRCh38#53968623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77301978-A-C

53970834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301849-A-G

53970834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301849-A-T

53970885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301801-G-C

53970970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301720-A-G

53971219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301528-G-A

53971219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301528-G-T

53971534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301175-A-G

53971580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301129-G-C

53971876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77300674-T-C

53971945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77300605-C-G

53971984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77300570-G-A

53972048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77300505-C-T

53972088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77300473-C-G

53976056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296557-A-G

53976094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296518-A-G

53976095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296517-A-G

http://identifiers.org/hco/6/GRCh38#53976116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77296496-A-C

53976116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296496-A-G

53976145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296477-G-T

53976151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296471-G-T

53976492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296181-G-T

53976512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77296161-A-G

53976779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77295931-G-A

53976823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77295869-G-T

53976931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77295770-G-A

53977247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77295552-G-A

53977247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77295552-G-T

53979265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294636-A-G

53979326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294572-T-C

53979342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294566-G-C

http://identifiers.org/hco/6/GRCh38#53979513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77294413-C-A

53979656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294229-A-T

53979760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294145-G-A

http://identifiers.org/hco/6/GRCh38#53981995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77293870-C-A

53981995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77293870-C-T

53982467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291810-T-C

53982470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291807-A-G

53982523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291748-G-A

53982634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291636-G-C

http://identifiers.org/hco/6/GRCh38#53982646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77291624-C-A

53982680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291590-T-A

53982680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291590-T-C

53982771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77291482-T-C

53982842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77291411-G-A

53982860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291389-A-T

53982909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291336-G-T

53983016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291109-T-G

53983126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290952-A-G

53983129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290949-T-C

53983193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290892-G-A

53983194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290891-T-C

53983755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290744-G-A

53983755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290744-G-T

53983890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290577-A-T

http://identifiers.org/hco/6/GRCh38#53984634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77289218-A-C

53984687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77289166-A-G

53984982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77288888-G-A

http://identifiers.org/hco/6/GRCh38#53985602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77287793-C-A

53985602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77287793-C-T

53985810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77287603-A-T

53985836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77287577-T-C

53986385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77287052-A-G

53986530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285679-C-T

53986627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285599-T-C

53986675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285536-G-T

53986821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285443-G-A

53986821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285443-G-T

53987095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285081-A-T

53987311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284877-C-T

53987473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284729-A-G

53987739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284522-G-A

53987740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284521-C-T

http://identifiers.org/hco/6/GRCh38#53987787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77284510-A-C

53987931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284449-A-G

53988230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284187-T-A

53988230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284187-T-G

53988284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284137-T-C

53988815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283574-T-A

53988815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283574-T-G

53988830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283559-T-G

53988949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283454-C-T

http://identifiers.org/hco/6/GRCh38#53988951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77283452-C-A

53988951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283452-C-T

53988970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283433-G-A

53988970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283433-G-T

53989055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283364-T-G

53989163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283247-T-A

53989214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283197-C-T

53989282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283133-A-G

53989375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283036-C-G

53989762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282741-C-G

53989762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282741-C-T

53989787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282716-A-G

53989866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282298-G-T

http://identifiers.org/hco/6/GRCh38#53989887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77282284-C-A

http://identifiers.org/hco/6/GRCh38#53989919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77282261-C-A

53989919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282261-C-T

53989991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282200-T-C

53990044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282150-G-A

53990198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282006-C-T

53990268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281955-C-T

53990304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281919-G-A

53990304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281919-G-T

53990524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281706-G-C

53990556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281632-T-G

53990686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281499-T-A

53990777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281426-T-A

53990799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281392-T-C

53993917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77278080-T-C

53994085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277941-A-G

53994171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277871-G-C

53994408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277650-C-T

53994545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277514-G-A

53994622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277426-T-G

53994638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277409-G-A

53994643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277404-G-A

53994643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277404-G-T

53994681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277373-G-T

53994698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277360-C-T

53995342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276961-C-T

53995415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276893-A-G

http://identifiers.org/hco/6/GRCh38#53995783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276563-C-A

53995783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276563-C-T

53995806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276541-T-A

53995862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276498-A-G

53995976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276412-T-C

http://identifiers.org/hco/6/GRCh38#53996047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276352-C-A

53996120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276289-T-C

http://identifiers.org/hco/6/GRCh38#53996142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276263-A-C

53996143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276262-T-C

53996188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276218-G-C

53996226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276183-G-A

53996288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276127-T-C

http://identifiers.org/hco/6/GRCh38#53996347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276077-C-A

http://identifiers.org/hco/6/GRCh38#53996374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276053-C-A

53996374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276053-C-T

53996578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275843-G-T

53996717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275694-G-A

53996729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275681-A-T

53996758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275656-A-G

53996795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275617-T-C

53996822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275590-G-A

53996863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275542-A-T

53996884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275521-A-G

53996884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275521-A-T

53996972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275458-T-C

53997057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275378-G-A

53997057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275378-G-T

53997092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275340-C-T

53997312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275101-T-C

53997322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275091-T-C

53997389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275028-G-A

53997674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274245-A-T

53997957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274001-A-G

53997964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273994-G-A

53997964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273994-G-T

53998073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273904-T-C

53998145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273825-C-T

53998250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273752-T-C

53998259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273747-A-G

53998286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273720-G-A

53998370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273636-C-T

53998495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273479-A-G

53998674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273232-G-C

53998752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273160-T-C

53998827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273084-G-A

53998827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273084-G-T

http://identifiers.org/hco/6/GRCh38#53999115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77272757-C-A

53999115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77272757-C-T

54000559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271445-T-A

54000559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271445-T-G

54000595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271415-G-A

http://identifiers.org/hco/6/GRCh38#54000779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77271238-C-A

54000813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271223-G-C

54000846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271190-T-A

54000846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271190-T-C

54000846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271190-T-G

54000870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271160-T-C

54000883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271149-G-T

54001041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77270994-C-T

http://identifiers.org/hco/6/GRCh38#54001115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77270923-C-A

54001461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270681-G-T

54001534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270615-G-A

54001742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270410-G-A

54001879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270294-A-G

54002087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270102-A-T

54002986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268226-T-C

54003045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268172-T-A

54003068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268159-G-C

54003068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268159-G-T

54003071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268153-T-C

http://identifiers.org/hco/6/GRCh38#54003106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77268117-A-C

54003141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268083-T-A

54003153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268071-G-A

http://identifiers.org/hco/6/GRCh38#54003155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77268069-A-C

54003474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77267888-G-T

http://identifiers.org/hco/6/GRCh38#54004327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77267352-C-A

54004809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266890-A-G

54004818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266881-A-G

54004844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266841-C-T

54004872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266813-G-A

54005328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266688-G-A

54007586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262648-G-A

54007586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262648-G-T

54007758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262476-A-G

54008603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262235-G-A

54008604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262234-G-T

54008764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262108-T-C

http://identifiers.org/hco/6/GRCh38#54008800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77262072-C-A

54008800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262072-C-G

54008859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262019-T-A

54009154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261652-G-A

54009157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261649-C-G

54009157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261649-C-T

54009265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261546-T-G

54009345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261484-G-T

54009986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260841-T-A

54010002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260822-C-T

54010506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260444-G-A

54010578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260371-T-G

54010612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260340-A-G

54010732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260244-A-T

54010772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260213-C-T

54010863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260123-C-G

54010866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260120-A-G

54011084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259910-A-G

54011153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259845-G-A

54011178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259801-C-T

54011407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259587-T-G

54011414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259580-G-A

54011437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259491-G-C

54011551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259386-A-G

54011602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259344-T-A

54011807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259154-T-C

54012064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258277-A-T

54012084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258257-A-T

54012144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258206-T-A

54012258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258105-A-G

http://identifiers.org/hco/6/GRCh38#54012366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77258002-A-C

54012497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257843-C-G

http://identifiers.org/hco/6/GRCh38#54012899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77257127-C-A

54012945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257081-T-C

54013214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256780-G-A

54013664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256391-G-C

54013758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256302-T-A

54017881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256160-G-T

54017915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256129-A-G

54018006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77256055-G-A

54018006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77256055-G-T

54018063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77256017-G-A

http://identifiers.org/hco/6/GRCh38#54018075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77256005-C-A

54018112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77255984-A-G

54018225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255863-G-T

54018904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255174-T-A

54018990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77255088-T-C

54019037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77255035-T-C

54019081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77254985-A-G

54019171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254893-T-C

54019225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254841-A-T

54019236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254831-G-A

54019236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254831-G-T

54019334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254734-T-G

54019561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254498-C-G

54019674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254387-C-T

54019965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254108-T-C

54020094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253991-G-A

54020319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253771-T-G

54020353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253643-C-T

54020358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253639-G-A

54020760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253270-T-C

54020826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253203-G-A

54020907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253120-G-A

54020950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253094-C-T

54021018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253025-A-G

54021343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252724-G-A

54021451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252632-A-G

54021696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252032-G-T

54021891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251855-G-A

54021999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251747-T-G

54022073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251679-T-G

54022096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251657-A-G

54022133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251619-A-G

54022319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251456-A-T

54022452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251327-G-C

54022783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251008-G-C

54022842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250947-C-T

54023247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250874-A-G

54023258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250863-A-G

54023446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250714-A-G

http://identifiers.org/hco/6/GRCh38#54023448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77250712-A-C

54024357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250476-A-G

54024505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250354-G-A

54024644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250242-T-C

54025312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249929-T-C

54025433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249843-G-T

http://identifiers.org/hco/6/GRCh38#54025566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77249754-A-C

54025566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249754-A-G

54025602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249717-T-A

54025638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249679-G-A

54025639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249678-T-A

54025639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249678-T-C

54025663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249648-C-T

54025689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249626-A-G

54025733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249593-T-A

54025780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249549-A-G

54026058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249275-G-A

http://identifiers.org/hco/6/GRCh38#54026071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77249262-C-A

54026088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249245-G-A

54026414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248927-T-C

54026415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248926-T-G

54026450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248892-G-T

54026609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248774-T-C

54026652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248734-G-A

54026652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248734-G-T

54026797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248645-C-T

54026845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248598-A-T

54026955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248492-C-T

54027049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248422-G-A

54027284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248188-G-A

54027284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248188-G-T

54027320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248155-C-T

54027512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248015-G-A

54027512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248015-G-T

54027581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247946-G-A

54027581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247946-G-T

54027942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247569-T-C

54027944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247564-C-T

54028026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247487-T-G

54028523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247018-G-A

54028579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246971-C-T

54028629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246923-T-C

54028652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246858-T-C

54028660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246850-C-T

54028734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246713-G-A

54028747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246700-A-G

54028747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246700-A-T

54028779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246679-T-C

54028864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246602-A-G

54028871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246592-T-A

54028888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77246580-T-C

54028943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77246534-G-A

54029216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245886-G-T

54029305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245795-T-C

54029309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245791-A-G

54029309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245791-A-T

54029316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245784-A-G

54029351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245750-G-A

54029351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245750-G-T

54029360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245741-G-A

54029360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245741-G-C

54029361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245740-A-G

54029361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245740-A-T

54029396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245726-A-G

54029396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245726-A-T

http://identifiers.org/hco/6/GRCh38#54029435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77245687-C-A

http://identifiers.org/hco/6/GRCh38#54029439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77245683-C-A

54029441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245681-T-C

54029475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245647-A-G

54029535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245564-T-C

54029588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245518-A-G

54029591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245515-G-C

54030375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244904-T-C

54030448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244852-G-A

54030487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244815-T-C

54030565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244713-C-T

http://identifiers.org/hco/6/GRCh38#54030677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77244577-C-A

54030721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244543-T-C

54030743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244530-G-T

54031392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243472-A-G

54031404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243459-C-T

54031449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243413-G-A

54031449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243413-G-T

54031493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243370-T-C

54031514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243348-G-T

54031537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243325-C-T

54031540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243322-G-T

54031658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77243131-C-G

54031658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77243131-C-T

54031971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242804-C-T

54031984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242768-C-T

54037640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77234503-T-C

54037778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234358-C-T

http://identifiers.org/hco/6/GRCh38#54037830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77234319-A-C

54037907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234257-A-G

54037944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234219-A-T

54038141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234033-G-A

54038143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234031-A-G

54038288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233888-G-A

54038502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233742-T-G

54038533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233713-T-C

54038616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233640-T-C

54038653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233600-A-G

54038706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233547-C-T

http://identifiers.org/hco/6/GRCh38#54039036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77233238-C-A

54039367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232915-G-A

54039367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232915-G-T

54039382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232899-G-A

54039382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232899-G-C

54039701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232566-G-A

54042240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77231211-G-A

54042419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77231026-G-T

54042482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230963-C-T

54042606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230817-T-C

54042633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230789-G-A

54042660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230762-G-A

54042700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230727-T-C

54042719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230708-G-A

54043535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77229527-A-G

54043540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77229522-G-T

54043947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227840-G-C

54044210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227458-T-G

54044220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227448-T-C

54044361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227320-C-T

54044646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227006-T-C

54044646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227006-T-G

54044665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77226988-A-G

54044665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77226988-A-T

54045011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77226042-T-G

54045468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225895-G-A

54045468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225895-G-C

54045521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225841-G-A

54046076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225741-T-A

http://identifiers.org/hco/6/GRCh38#54046126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225693-C-A

http://identifiers.org/hco/6/GRCh38#54046127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225692-C-A

54046127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225692-C-G

54046127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225692-C-T

http://identifiers.org/hco/6/GRCh38#54046208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225616-A-C

54046239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225594-A-G

http://identifiers.org/hco/6/GRCh38#54046265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225575-C-A

54046265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225575-C-T

54046345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225490-A-G

http://identifiers.org/hco/6/GRCh38#54046693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77224895-C-A

54046733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77224852-T-C

54046734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77224851-G-A

http://identifiers.org/hco/6/GRCh38#54046744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77224841-C-A

54046982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77224620-G-T

54047212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77224438-A-G

54047244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77224407-A-G

54047292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77224356-C-T

http://identifiers.org/hco/6/GRCh38#54047312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77224318-C-A

54047541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77223523-T-A

54047541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77223523-T-C

54048186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77223201-T-G

54048232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77223146-T-C

54048610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77223028-T-C

54048917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222681-T-G

54049250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222425-T-C

54049307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222368-A-T

54049441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222236-G-T

54049564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222127-C-G

54049607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222085-C-G

54049682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221993-C-T

54050657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220597-A-T

54050738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220520-G-T

54050968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220306-G-A

54050977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220297-C-T

http://identifiers.org/hco/6/GRCh38#54050995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77220280-C-A

http://identifiers.org/hco/6/GRCh38#54050999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77220276-C-A

54051214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220100-T-C

http://identifiers.org/hco/6/GRCh38#54051283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77220042-C-A

54051582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219738-A-T

54051595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219687-T-G

http://identifiers.org/hco/6/GRCh38#54051693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77219595-C-A

54051693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219595-C-T

54051779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219525-A-T

54051962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219302-T-C

54052053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219210-T-C

54053143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219162-T-C

54053198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219109-G-A

54053291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219021-A-T

54053433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218876-T-C

http://identifiers.org/hco/6/GRCh38#54053648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77218629-A-C

54053680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218593-T-C

54053764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218512-A-G

54054187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218090-C-T

54054220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218058-C-T

54054421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217858-A-G

54054431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217848-A-T

54054457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217825-C-G

54054478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217803-A-G

54054486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217795-T-C

54055221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217010-T-C

http://identifiers.org/hco/6/GRCh38#54055224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77217007-A-C

54055224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217007-A-G

54055641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216508-G-C

54055749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216387-A-G

54055796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216339-G-A

http://identifiers.org/hco/6/GRCh38#54056329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77215801-A-C

54056329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215801-A-T

54056559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215581-T-C

54056587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215553-G-A

54056610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215530-A-G

54056677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215463-C-G

54056835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215320-A-G

54057036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215136-T-C

54057071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215101-T-C

54057255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214921-A-G

54057270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214905-G-A

54057437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77213906-G-A

54057553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77213791-A-G

54058822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212942-C-T

54058826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212938-A-G

http://identifiers.org/hco/6/GRCh38#54058933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77212865-A-C

54058933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77212865-A-T

54058953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77212851-A-G

54058971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 77212833-C-T

http://identifiers.org/hco/6/GRCh38#54059001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77212809-A-C

54059314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211532-T-C

54059374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211498-A-G

54060021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210959-A-G

54060023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210957-G-A

54060023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210957-G-T

54060224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210762-G-T

54060617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210395-T-A

54060643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210363-G-A

54061030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209991-C-T

54061275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209774-G-A

54061288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209761-A-G

http://identifiers.org/hco/6/GRCh38#54061641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77209034-C-A

54061823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208872-C-T

54061824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208871-T-C

54061846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208855-G-A

54062109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208586-T-C

54062175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208523-A-G

54062186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208512-A-G

54063757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208232-G-A

54063757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208232-G-T

54063905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208101-A-G

54064751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77206096-T-G

54067144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77204912-G-A

54067171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77204853-T-C

54068778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77203832-A-T

http://identifiers.org/hco/6/GRCh38#54068955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77203638-A-C

54068955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77203638-A-G

54069980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202579-C-G

54070067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201326-C-T

54070117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201285-T-C

54070160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201248-T-C

54070230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201174-C-T

54070358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201046-T-A

54070358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201046-T-C

54070426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200979-G-T

54070499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200916-T-C

54072672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200050-C-T

54073201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199521-T-C

http://identifiers.org/hco/6/GRCh38#54073351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77199415-A-C

54074070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198844-C-T

54074163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198762-T-G

54074220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198704-G-A

54074363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198562-G-A

54074373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198552-T-A

54074506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198411-A-G

54074588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198327-G-A

54074588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198327-G-T

54074822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198086-A-G

54075011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197946-G-T

54075675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197601-G-A

54075755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197544-G-T

54075804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197510-C-T

54075818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197496-T-C

54075914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197401-T-G

54076374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196958-A-G

54076471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196888-A-G

54076590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196775-T-C

54076669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196705-T-C

54076752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196179-A-G

54076762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196169-T-G

54076891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196043-A-G

54077034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195851-A-G

54077261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195635-A-G

54077276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195620-A-G

54077348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195554-A-G

54077372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195530-T-C

54078233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194835-C-T

54079903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77191530-C-T

http://identifiers.org/hco/6/GRCh38#54080270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77191222-C-A

54080446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77191033-T-C

54080524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190970-G-A

54080524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190970-G-T

54080557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190938-A-G

54080902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190809-T-G

http://identifiers.org/hco/6/GRCh38#54080928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77190780-C-A

54080977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190727-G-T

54080993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190711-C-G

54081009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190697-A-T

54081038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190667-T-G

54081124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77190579-C-T

54083335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186719-G-A

54083335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186719-G-T

54083350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186699-T-C

54083424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77186636-G-A

54083488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77186572-G-C

54083632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186446-T-G

54083775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186321-G-A

54083809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186291-C-G

54083955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77186132-G-A

54084049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77185974-T-C

54084257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77185720-G-T

54084416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77185588-C-T

54084524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77185482-A-G

54084570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77185426-G-A

54084975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77185017-T-C

http://identifiers.org/hco/6/GRCh38#54085003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77184992-A-C

54085263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77184771-T-C

54085265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77184769-A-G

54085526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77184474-G-C

54085559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77184435-A-G

54085633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77184362-G-A

54086041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77183979-G-A

54086265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77183791-T-A

54086384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77183679-A-G

54087154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77182247-T-C

54087268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77182187-G-A

http://identifiers.org/hco/6/GRCh38#54087373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77182096-A-C

54087916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77181798-C-T

54087966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77181749-C-T

54088027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77181696-C-T

54088416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77180025-C-T

54088473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179996-T-G

54088567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179902-G-A

54088603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179867-T-G

54088619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179851-G-A

54088634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179836-C-T

54088693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179763-T-C

54088874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179643-G-A

54088880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179637-T-G

54088921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179558-C-G

54088927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179552-G-A

54088970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179471-A-G

54089311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77179025-C-T

54089664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178723-T-C

54089723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178665-G-A

http://identifiers.org/hco/6/GRCh38#54089883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77178500-A-C

54089920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178465-G-A

54089986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178395-C-T

54090048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178334-T-A

54090113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178293-A-G

54090113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178293-A-T

54090269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178153-A-G

54090307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77178116-T-G

54090528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77177170-C-T

54090581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77177119-C-T

54090691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77177043-G-A

54090748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176993-A-G

54090944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176842-A-G

54091035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176747-A-G

54091225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176586-C-T

54091234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176577-T-C

54091300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176512-T-C

54091554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77176204-G-T

54091846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77175925-T-G

54092123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77175679-A-G

54092249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77175549-G-A

54092305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77175493-C-T

54092316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77175482-G-A

54092516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77174877-A-G

54092708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77174756-A-T

54092826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77174659-T-C

54093297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77174517-T-C

54093438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77174430-T-C

54093826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77174072-T-G

54094138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173795-C-G

54094216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173720-A-G

54094231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173693-C-T

http://identifiers.org/hco/6/GRCh38#54094246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77173678-C-A

54094381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173552-A-G

54094422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173506-T-C

54094507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173426-T-C

54094523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173410-G-A

54094570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77173362-T-C

http://identifiers.org/hco/6/GRCh38#54094831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77173124-C-A

54095061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77172897-A-G

54095456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77172516-C-G

54095621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77172361-C-T

http://identifiers.org/hco/6/GRCh38#54095634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77172348-A-C

54095745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77172227-A-G

54095748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77172224-A-G

54096180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77171928-T-A

54096180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77171928-T-C

54096371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77171744-G-A

54096449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77171669-G-T

54096650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77171465-G-C

http://identifiers.org/hco/6/GRCh38#54096663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77171452-C-A

54096896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170979-G-A

54097059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170804-A-G

http://identifiers.org/hco/6/GRCh38#54097413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77170465-C-A

54097413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170465-C-T

54097451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170425-C-T

54097455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170421-T-G

54097520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170355-C-G

54097683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, undefined
orthologous variants: 77170228-A-G

54097720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77170190-A-G

54097820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, undefined
orthologous variants: 77170094-G-T

54097925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, undefined
orthologous variants: 77170005-A-G

54097925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, undefined
orthologous variants: 77170005-A-T

54099367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77168906-C-G

54099547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77168726-G-A

54099547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77168726-G-T

54099657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77168626-G-A

54099657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77168626-G-T

54099841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77168434-C-T

54100106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77168184-T-A

54100640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77167879-T-A

54100648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77167871-C-T

54100720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77167812-T-C

54100838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77167682-G-C

54100959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77167589-C-T

54101426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77167273-T-C

http://identifiers.org/hco/6/GRCh38#54102002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77166589-C-A

54102202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77166394-G-A

54102791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77165882-T-C

54103048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77165634-T-G

54108679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77161780-T-C

54108706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77161750-T-C

54108756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77161698-G-A

http://identifiers.org/hco/6/GRCh38#54109248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77161323-A-C

http://identifiers.org/hco/6/GRCh38#54109278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77161293-A-C

54109424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77161170-G-A

54109477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77161135-C-T

54109603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77161018-T-C

54110351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77160335-T-C

54110389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77160310-T-C

http://identifiers.org/hco/6/GRCh38#54111152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77159547-C-A

http://identifiers.org/hco/6/GRCh38#54111307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77159412-C-A

54111307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77159412-C-G

54111347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77159380-A-G

54111355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77159372-A-T

54111400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77159175-A-T

54111496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77159106-G-A

http://identifiers.org/hco/6/GRCh38#54111669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77158940-C-A

54111669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77158940-C-T

http://identifiers.org/hco/6/GRCh38#54111864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77158740-C-A

54111984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77158617-C-T

54111990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77158607-G-A

54112739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77157749-A-G

54112792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77157696-G-A

54120968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77152262-T-A

http://identifiers.org/hco/6/GRCh38#54121420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77151034-A-C

54121561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77150893-C-G

54121561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77150893-C-T

54121581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77150873-G-A

54121668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150786-G-A

54121739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150615-T-C

54121767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150520-T-A

54121767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150520-T-C

54121790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150444-T-C

54121825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150410-G-T

54121941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150270-A-G

54121953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150254-T-C

54122086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150139-C-T

54122153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77150102-T-C

54122319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77149937-G-A

54122438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77149661-T-A

54122710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77149377-T-C

54123365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148943-G-A

54123459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148852-T-C

54123472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148836-T-C

54123488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148817-A-G

54123648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148676-C-T

54123756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148578-A-G

54123756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77148578-A-T

54123964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147585-C-T

http://identifiers.org/hco/6/GRCh38#54123965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77147584-C-A

54124034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147510-G-A

54124043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147504-T-A

http://identifiers.org/hco/6/GRCh38#54124199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77147343-A-C

54124352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147193-G-C

54124352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147193-G-T

54124359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147186-T-C

54124359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147186-T-G

http://identifiers.org/hco/6/GRCh38#54124402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77147137-A-C

54124402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77147137-A-G

54124537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 77147000-T-A

http://identifiers.org/hco/6/GRCh38#54124545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77146992-C-A

54124545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77146992-C-T

54124597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77146940-A-T

54124709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77146828-G-A

54124709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77146828-G-T

54124819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77146718-A-G

54124862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77146675-G-A

54124862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77146675-G-T

54124975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146583-G-A

54124975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146583-G-T

http://identifiers.org/hco/6/GRCh38#54124980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77146578-A-C

54124980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146578-A-G

54125023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146537-G-C

54125216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146389-G-A

54125355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146244-A-G

54125468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146130-A-G

54125604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77146008-A-G

54125719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145911-A-G

54125960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145670-C-T

54126113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145137-A-G

54126147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77145103-G-T

54128971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77143940-G-A

http://identifiers.org/hco/6/GRCh38#54129014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77143895-C-A

54129277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77143504-T-C

54129332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77143468-A-T

54129612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77143203-A-G

54130231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142805-G-A

54130290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142748-G-A

54130290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142748-G-C

54130290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142748-G-T

54130301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142737-G-A

54132275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142227-A-T

54132331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142172-T-A

54132379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142121-G-A

http://identifiers.org/hco/6/GRCh38#54132406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77142094-C-A

54132422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77142078-C-T

http://identifiers.org/hco/6/GRCh38#54132623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77142021-A-C

54132863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141830-G-A

54132992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141725-T-G

54133020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141711-G-A

54133227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141524-A-G

54133348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141404-A-G

54133425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141336-C-T

54133505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141281-T-C

54133690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141122-T-G

54133716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77141096-T-C

54133879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140951-T-C

54133945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140899-A-G

54134231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140702-T-C

54134247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140684-T-G

54134471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140514-G-A

54134845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140197-C-T

54134898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140137-A-G

54134937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77140102-G-A

http://identifiers.org/hco/6/GRCh38#54135247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77139767-A-C

54135643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77139389-A-G

54135719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77139252-T-A

54135719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77139252-T-C

54135785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77139199-A-T

54136160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77138858-T-C

http://identifiers.org/hco/6/GRCh38#54136483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77138538-C-A

54136500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77138521-G-A

54136575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77138451-A-T

54136718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138306-A-G

54136815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138212-A-G

54136826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138201-G-A

54136826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138201-G-T

54136906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138121-A-T

http://identifiers.org/hco/6/GRCh38#54136925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77138102-C-A

54136925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138102-C-T

54136962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77138068-T-C

54137415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137621-T-G

54137451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137585-C-G

54137451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137585-C-T

54137498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137538-G-A

54137498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137538-G-T

54137586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137453-C-G

54137586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137453-C-T

54137657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137382-A-G

http://identifiers.org/hco/6/GRCh38#54137678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77137361-C-A

54137678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137361-C-T

http://identifiers.org/hco/6/GRCh38#54137737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77137299-C-A

54137737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77137299-C-T

54137784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137252-G-A

54137784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137252-G-T

54137809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137227-C-G

54137809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77137227-C-T

http://identifiers.org/hco/6/GRCh38#54137912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77137142-C-A

54137912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77137142-C-T

54137977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77137074-G-A

http://identifiers.org/hco/6/GRCh38#54138059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77136992-C-A

54138059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77136992-C-T

54138060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77136991-A-T

54138106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77136945-G-A

54138328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77136722-A-G

http://identifiers.org/hco/6/GRCh38#54138364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77136709-C-A

54138675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77136412-C-G

54138675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77136412-C-T

54138788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135949-T-C

54138788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135949-T-G

54138803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135934-G-A

54138860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135877-T-C

54138863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135874-A-G

54138915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135822-G-A

54139098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135641-G-C

54139104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77135635-T-C

http://identifiers.org/hco/6/GRCh38#54139126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77135613-C-A

54140411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77134653-T-G

54141136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133914-T-C

54141724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133657-T-C

54141761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133617-A-G

54142062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133336-C-T

54142142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133266-G-A

54142257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133188-A-G

54142337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133121-A-G

54142405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133056-T-C

54142417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77133044-T-C

54144075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77129426-T-C

54147265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77128467-G-T

54147444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77128317-T-A

54147474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77128288-T-C

54147489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77128275-C-T

54147743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77128020-A-G

54147803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77127945-T-G

54147962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77127806-G-C

54148361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124989-G-A

54148436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124917-G-A

54148467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124888-G-C

54148534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124836-T-A

54148869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124512-C-T

54148930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124450-G-T

http://identifiers.org/hco/6/GRCh38#54148934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77124449-A-C

http://identifiers.org/hco/6/GRCh38#54148945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77124438-C-A

54148945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124438-C-T

54149208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124174-A-G

54149279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124107-A-G

54149279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77124107-A-T

54149507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123910-G-T

http://identifiers.org/hco/6/GRCh38#54149582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77123839-A-C

54149582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123839-A-G

http://identifiers.org/hco/6/GRCh38#54149869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77123578-C-A

54149879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123568-G-T

54150054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123384-A-G

54150174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123266-G-A

54150346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123057-T-C

54150346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123057-T-G

54150357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123046-T-C

54150394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77123026-G-A

54150510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77122923-G-T

http://identifiers.org/hco/6/GRCh38#54150723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77122741-A-C

54150750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77122715-A-G

54150906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77121465-G-A

54151054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77121331-G-A

54151194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77121195-C-T

54151762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77115451-A-G

54151769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77115444-A-G

54151952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77115268-T-C

54152775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77114776-T-C

54152863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77114688-G-C

54153124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77114421-A-G

54153126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77114419-C-G

54153282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77114233-G-T

http://identifiers.org/hco/6/GRCh38#54153490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77114179-A-C

http://identifiers.org/hco/6/GRCh38#54153513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77114157-C-A

http://identifiers.org/hco/6/GRCh38#54153936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77114061-C-A

54153989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77114035-A-G

54154823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77105384-G-A

54154823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77105384-G-C

54154948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77105258-A-G

54155112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77105053-A-G

54156705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77103861-A-G

54157027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77103280-A-T

54157126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77103189-C-T

54157131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77103184-G-A

54157242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77103015-C-G

54157353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77102909-C-T

54157364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77102898-C-T

54157602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77102649-T-C

54158086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77101967-T-C

54158098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77101955-A-G

54158411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77101638-T-C

54158624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77099838-A-T

54158768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77099664-G-A

54158768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77099664-G-T

54158841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77099571-T-C

http://identifiers.org/hco/6/GRCh38#54160328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77098056-C-A

54160413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77097971-C-T

54160880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77097525-T-C

54160913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77097492-A-G

54161015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77097432-A-G

54161204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77097236-G-A

54161625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096846-G-A

54162405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096405-G-C

54162406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096404-G-A

54162470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096354-G-A

54162523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096332-T-A

54162577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096275-G-C

54162791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096083-G-A

54162807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096062-A-G

54162860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096012-C-T

54162866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77096006-A-G

54162951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77095925-T-C

54163142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77095749-T-C

54163199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77095699-T-C

54163321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77095403-A-G

54163374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77095348-G-T

http://identifiers.org/hco/6/GRCh38#54165275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77091813-C-A

54165339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77091756-G-A

54165855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77091228-G-T

54165899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77091193-C-G

54165966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77091121-C-T

54166131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090970-G-A

54166134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090967-A-G

54166511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090499-C-T

54166604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090418-C-G

54166638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090384-G-A

54166639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090383-T-C

http://identifiers.org/hco/6/GRCh38#54166882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77090159-C-A

54166884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090157-A-G

54166962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090084-T-C

54167030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090030-T-C

54167031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77090029-A-T

54167087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77089971-G-A

54167273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77089804-T-C

54168772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77089466-A-G

54168887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77089357-G-A

54168887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77089357-G-T

54168888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77089356-T-G

54169270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088943-T-A

54169270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088943-T-C

54169399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088812-T-G

54169451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088753-G-A

54169451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088753-G-T

54169509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088695-T-A

54169570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77088634-T-C

http://identifiers.org/hco/6/GRCh38#54169638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77088566-C-A

54169650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088554-G-A

54169660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088540-T-C

54169660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088540-T-G

54169691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77088506-G-A

54170382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77087063-G-T

54170888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77086572-T-C

54171007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77086428-T-A

54171024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77086411-C-T

http://identifiers.org/hco/6/GRCh38#54171039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77086389-A-C

54171146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77086288-G-C

54171358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77085780-A-G

http://identifiers.org/hco/6/GRCh38#54171511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77085618-C-A

54171756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77085387-A-G

54171765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77085378-T-A

54171765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77085378-T-C

54172032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77085136-C-G

54172055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77085113-T-A

54172348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084949-A-G

54172541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084773-C-G

54172715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084595-A-G

54172719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084591-G-A

54172719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084591-G-C

54172727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084583-T-A

54172727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084583-T-G

http://identifiers.org/hco/6/GRCh38#54172731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77084579-C-A

54172731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084579-C-G

54172735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084575-G-A

54173014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084200-T-C

54173049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77084167-T-C

http://identifiers.org/hco/6/GRCh38#54182636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77083909-C-A

54182708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77083851-T-C

54182809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77083749-A-G

54182819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77083739-C-T

54183139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77083403-C-T

http://identifiers.org/hco/6/GRCh38#54183165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77083377-A-C

http://identifiers.org/hco/6/GRCh38#54183329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77083219-A-C

54183371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77083178-T-C

54188822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77082267-A-G

54189105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77082010-G-A

54189114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77081999-G-A

54189802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77081348-A-T

54189900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77081253-T-C

54189919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77081234-G-A

54189919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77081234-G-T

http://identifiers.org/hco/6/GRCh38#54189951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77081217-C-A

54189978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77081191-G-A

54189978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77081191-G-T

54189993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77081177-A-G

54189993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77081177-A-T

54189995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77081175-A-G

54189995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77081175-A-T

54193292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77080454-A-T

http://identifiers.org/hco/6/GRCh38#54193624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77080125-A-C

54193835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77079925-G-A

54193943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77079824-G-A

54194078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77079688-C-T

54194184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77079584-T-G

54194353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77079438-G-A

54194578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77079219-T-G

54194888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77078996-A-G

54194978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77078922-G-T

54195216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77078697-G-A

54195498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77078393-G-A

54195701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77078188-A-G

54195790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77078074-T-A

54196845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77077171-G-A

http://identifiers.org/hco/6/GRCh38#54197039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77077021-A-C

http://identifiers.org/hco/6/GRCh38#54197053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77077007-A-C

54197060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77077001-A-G

54197094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076945-T-C

54197206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076872-A-T

54197431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076669-C-G

54197508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076593-T-C

54197541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076559-A-G

54197592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076528-C-T

54197797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076346-A-G

54197891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77076252-T-G

http://identifiers.org/hco/6/GRCh38#54198777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77075211-A-C

54199159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77074931-T-C

http://identifiers.org/hco/6/GRCh38#54199326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77074784-A-C

54199804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77074410-G-A

http://identifiers.org/hco/6/GRCh38#54200070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77074153-C-A

54200366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77073616-A-T

54200461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77073554-C-T

54200713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77073399-T-A

54200803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77073311-T-C

http://identifiers.org/hco/6/GRCh38#54201155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77072957-C-A

54201155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072957-C-G

54201352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072799-T-A

54201352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072799-T-C

54201512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072667-C-T

http://identifiers.org/hco/6/GRCh38#54201858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77072443-C-A

54201862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072439-T-C

54201864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072437-G-C

54201888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072414-T-C

http://identifiers.org/hco/6/GRCh38#54202015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77072255-C-A

54202015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77072255-C-T

http://identifiers.org/hco/6/GRCh38#54202098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77072180-C-A

54202098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77072180-C-T

54202115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77072163-G-A

54202115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77072163-G-T

54202201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77072077-T-C

54202376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071958-G-T

54202515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071812-G-A

54202515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071812-G-T

54202517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071810-A-T

54203186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071191-C-T

54203349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77070981-C-G

54203509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77070833-A-G

54203561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77070784-T-G

54203958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77070707-A-G

http://identifiers.org/hco/6/GRCh38#54204073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77070591-A-C

54204336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77070258-G-C

54204343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77070251-T-G

54204452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77070144-A-G

54204593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77070005-C-T

54204747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77069855-T-A

54204774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77069828-A-G

54204854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, undefined
orthologous variants: 77069744-T-C

54205065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77069549-G-A

54205207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77069405-G-A

54205423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77069198-C-T

54205482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77069139-T-A

http://identifiers.org/hco/6/GRCh38#54205483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77069138-C-A

54205648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77068976-A-G

54205730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77068892-A-G

54206458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77068235-T-C

54206521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77068173-T-C

54206521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77068173-T-G

54207028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77067552-T-C

54207445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77067176-A-T

54207537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77067083-A-G

54214596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77057586-G-A

54214596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77057586-G-T

54214709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77057471-T-G

54214731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77057449-A-G

54214834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77057364-G-A

54215938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056836-G-T

54216129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056645-T-A

54216209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056547-A-G

54216424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056353-G-C

54216424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056353-G-T

54216498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056285-G-T

54216671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056141-C-T

54216703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056111-T-C

54216753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056081-C-T

http://identifiers.org/hco/6/GRCh38#54216774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77056060-A-C

54216774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056060-A-G

54216801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77056025-A-G

54216844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055983-T-C

54217101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055777-A-G

54217101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055777-A-T

54217112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055767-G-A

54217132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055757-T-C

54217175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055730-C-T

54217191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055713-C-T

54217233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055675-T-C

http://identifiers.org/hco/6/GRCh38#54217348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77055559-C-A

54217348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055559-C-T

http://identifiers.org/hco/6/GRCh38#54217436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77055479-A-C

54217436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055479-A-G

54217522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055393-T-C

54217574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055342-G-A

54217774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055141-A-G

54217941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77055000-G-T

54218094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77054861-C-T

54228464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047669-A-G

54228464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047669-A-T

54228505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047628-A-G

http://identifiers.org/hco/6/GRCh38#54228538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77047595-C-A

54228538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047595-C-G

54228668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047505-A-G

54228739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047438-C-G

54228739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047438-C-T

54228792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047389-A-T

http://identifiers.org/hco/6/GRCh38#54229079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77047157-C-A

54229079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047157-C-T

54229110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047139-G-A

54229138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047111-T-C

54229185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77047062-C-T

54229407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046860-T-A

54230024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046444-A-G

54230084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046397-G-A

54230084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046397-G-T

54230419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046092-A-G

54230420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046091-C-T

54230422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046089-G-A

54230482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77046029-G-T

54230544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045970-C-G

54230660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045885-G-A

54230660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045885-G-T

54230835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant
orthologous variants: 77045715-G-A

54230883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant
orthologous variants: 77045664-C-T

54231016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045526-T-C

54231026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045516-T-A

54231040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045502-G-A

54231152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045386-T-C

54231184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045354-T-C

54231187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045351-T-C

54231214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045324-C-T

54231253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045285-T-C

54231315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045227-G-C

54231346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77045199-C-T

54231756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044678-C-T

54231760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044674-C-T

54231916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044524-C-G

54231916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044524-C-T

54231954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044489-G-C

54232074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044382-C-T

54232293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77044186-A-G

http://identifiers.org/hco/6/GRCh38#54232713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77043657-A-C

54233017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77043380-C-T

54233049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77043356-T-C

54233057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77043347-T-G

http://identifiers.org/hco/6/GRCh38#54234374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77042879-A-C

54234374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77042879-A-G

54234437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77042820-T-C

http://identifiers.org/hco/6/GRCh38#54234515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77042741-C-A

54234532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77042721-T-A

54235209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77041491-A-G

54235224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77041475-T-C

54235288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77041411-G-A

http://identifiers.org/hco/6/GRCh38#54235300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77041399-C-A

54235369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77041333-G-A

54235522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77036532-G-T

http://identifiers.org/hco/6/GRCh38#54235547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77036505-C-A

54238334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035929-A-G

54238369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035892-A-T

http://identifiers.org/hco/6/GRCh38#54238415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77035848-A-C

54238436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035827-C-T

54238486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035781-T-C

54238691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035628-A-G

54238693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035626-G-A

54238693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035626-G-T

54238829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035509-T-A

54239109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035239-G-C

54239138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035200-A-G

54239187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77035098-A-G

54239312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77034979-C-T

54239944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77034728-T-C

54240212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77034532-T-G

54243948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77033552-A-G

54244649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, undefined
orthologous variants: 77032688-G-A

54247344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029733-A-G

http://identifiers.org/hco/6/GRCh38#54247370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77029707-A-C

54247383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029698-A-G

54247407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029674-G-T

54247447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029634-C-T

54247496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029580-C-T

54247537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029555-T-C

54247586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029510-C-G

54247680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029420-T-A

54247756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029345-C-G

http://identifiers.org/hco/6/GRCh38#54247774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77029327-C-A

54247907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029186-A-G

http://identifiers.org/hco/6/GRCh38#54247936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77029157-C-A

54247984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029125-G-A

54248012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029097-T-A

54248040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029069-G-A

54248042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029067-A-G

54248042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77029067-A-T

54248182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028933-A-G

54248303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028809-T-A

54248457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028653-A-G

http://identifiers.org/hco/6/GRCh38#54248521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77028589-C-A

54248568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028544-A-G

54248578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028534-A-G

54248678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028472-G-T

54248732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028422-A-G

54248934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028250-G-A

54249178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77028004-G-A

54249414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77027529-A-G

54249529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77027396-A-G

http://identifiers.org/hco/6/GRCh38#54250711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77027097-C-A

54250711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77027097-C-G

54250728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77027080-T-A

54250797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77027015-T-G

54250844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026980-A-G

54250870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026953-A-G

54250897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026926-G-T

54250915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026908-C-T

54250922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026901-C-G

54251291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026165-C-T

54251406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77026061-G-T

54253708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77024418-T-C

54253904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77024229-A-G

54254807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77023559-C-T

54254883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77023489-T-A

http://identifiers.org/hco/6/GRCh38#54254945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77023432-C-A

54254945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77023432-C-T

54255601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77022067-G-T

54255607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77022061-T-C

54255627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77022043-A-G

54255718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021954-G-T

54255727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021945-T-C

54255774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021900-T-C

54255816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021857-G-C

54255891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021783-A-T

http://identifiers.org/hco/6/GRCh38#54255963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77021712-A-C

54256023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021654-T-C

54256058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021619-T-G

54256395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021326-A-G

54256395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021326-A-T

http://identifiers.org/hco/6/GRCh38#54256403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77021318-C-A

54256479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021252-T-A

http://identifiers.org/hco/6/GRCh38#54256538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77021179-C-A

54256538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021179-C-T

54256549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77021118-T-G

54256929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77020684-A-G

54256934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77020679-C-G

54256936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77020677-T-C

54257382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77020234-G-C

54259551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: -G-A

http://identifiers.org/hco/6/GRCh38#54259670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77017269-C-A

54259670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77017269-C-T

54259681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77017258-A-G

54259797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77017148-T-C

54259837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77017108-A-G

54259931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77017031-A-G

54261078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77016467-C-T

54261241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77016210-C-T

54261429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77016060-C-T

54261452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77016037-A-G

http://identifiers.org/hco/6/GRCh38#54261470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77016019-A-C

http://identifiers.org/hco/6/GRCh38#54261635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77015627-A-C

54261635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 77015627-A-T

54261648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77015614-G-A

54261672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77015594-C-T

54261805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77015480-G-A

54261997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77015295-T-C

54262038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77015257-T-C

54262042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77015253-T-G

54262067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77015231-G-A

54262929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77014283-G-A

54263650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77011739-T-A

http://identifiers.org/hco/6/GRCh38#54263711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77011678-C-A

54264224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77011206-G-A

54264536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77010946-T-C

54264805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77010693-T-C

54265418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77010076-A-G

54265437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77010057-T-C

54265483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77010009-T-A

54265486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77010006-T-C

54265561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77009930-G-A

54265823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: intron variant
orthologous variants: 77009773-T-C

54265958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009665-T-C

54265987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009638-T-C

http://identifiers.org/hco/6/GRCh38#54266014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77009608-C-A

54266014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009608-C-T

http://identifiers.org/hco/6/GRCh38#54266103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77009532-C-A

54266103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009532-C-T

54266104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009531-T-C

54266107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009528-A-G

54266130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009505-T-C

http://identifiers.org/hco/6/GRCh38#54266177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77009460-C-A

54266177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21355
most severe consequence: 3 prime UTR variant
orthologous variants: 77009460-C-T