http://identifiers.org/hco/13/GRCh38#77026859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103336630-C-A

http://identifiers.org/hco/13/GRCh38#77026933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103336713-C-A

77026933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 103336713-C-T

http://identifiers.org/hco/13/GRCh38#77026988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103336768-C-A

77026988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 103336768-C-G

77027068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103336863-T-C

77027153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103336957-C-T

77027272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103337048-G-T

77027311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337081-T-G

77027757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337462-A-G

77027765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337470-G-A

77027820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337516-G-C

http://identifiers.org/hco/13/GRCh38#77027862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103337585-C-A

77027862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337585-C-T

77027883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337608-G-A

77027883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103337608-G-T

77027975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103337700-G-A

77027975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103337700-G-T

77027980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103337705-T-C

77039454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339126-A-G

77039529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339189-G-A

77039711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339366-G-C

77039711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339366-G-T

77039747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339394-C-T

77039833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339501-G-A

77039833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339501-G-T

77040052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339729-C-G

77040230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339881-C-G

77040230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103339881-C-T

77040344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103340015-A-G

77040350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103340021-G-A

http://identifiers.org/hco/13/GRCh38#77040428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103340091-C-A

77040428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103340091-C-T

77041532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103341249-G-A

http://identifiers.org/hco/13/GRCh38#77041559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103341280-A-C

77041574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103341295-C-T

77044513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103350734-C-T

77044566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103350782-T-C

77045049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351234-G-A

77045078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351263-T-C

77045104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351289-A-G

http://identifiers.org/hco/13/GRCh38#77045123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103351308-C-A

77045123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351308-C-T

77045194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351377-G-A

77045226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351408-T-C

77045438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351616-T-C

77045462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103351640-T-C

77045751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103351911-G-A

77045757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103351917-C-T

77045844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103351969-G-T

77045904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103352042-T-C

77048826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103352672-C-T

77048910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103352753-T-C

77049029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103352863-C-T

77049083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103352937-C-T

77050179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103353596-G-A

77050179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103353596-G-C

http://identifiers.org/hco/13/GRCh38#77050541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103353915-A-C

77050667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354051-T-C

77050845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354321-T-A

77050916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354390-G-A

77050916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354390-G-T

77051193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354685-A-G

77051193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354685-A-T

77051235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354732-A-G

77051235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103354732-A-T

77051513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103355009-A-T

http://identifiers.org/hco/13/GRCh38#77051692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103355173-C-A

77051692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103355173-C-T

http://identifiers.org/hco/13/GRCh38#77051778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103355277-A-C

77051778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103355277-A-G

77051778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103355277-A-T

77051877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103355543-T-G

77051883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103355549-C-G

77051883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103355549-C-T

77051935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355601-T-A

77051935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355601-T-C

77051935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355601-T-G

77051977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355627-T-C

http://identifiers.org/hco/13/GRCh38#77052066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103355684-C-A

77052066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355684-C-T

77052116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355726-C-T

77052318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103355787-C-T

77052703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103356056-T-A

77052703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103356056-T-C

77053494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103356504-C-T

77053770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103356782-C-T

77054031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357041-G-A

77054328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357260-A-G

77054358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357290-C-T

77055019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357548-C-T

77055126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357649-G-A

77055344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357738-T-C

77055436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357822-G-A

77055436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357822-G-C

77055436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357822-G-T

77055513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357899-G-A

77055513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357899-G-C

77055513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103357899-G-T

77055885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358267-T-G

77055975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358343-C-T

http://identifiers.org/hco/13/GRCh38#77056065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103358431-C-A

77056188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358509-C-T

77056399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358764-T-C

77056427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358790-G-C

http://identifiers.org/hco/13/GRCh38#77056844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103359817-C-A

77056844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103359817-C-G

77056844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103359817-C-T

77056887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103359860-G-T

77057004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103359969-T-C

77057004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103359969-T-G

77057110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360075-A-G

77057114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360079-G-T

77057145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360110-T-A

77057145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360110-T-C

77057447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360350-T-C

77057756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360604-C-G

77057988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103360622-C-T

77058272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103360802-A-G

77058329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103360859-A-G

77058359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103360889-T-A

77058359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103360889-T-C

77058437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103360967-G-A

77058496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103361026-C-T

77058543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103361069-G-T

http://identifiers.org/hco/13/GRCh38#77059286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103361656-A-C

77059430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103361732-G-A

77059430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103361732-G-C

77059430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103361732-G-T

77059504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103361813-T-C

77059630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 103361942-G-A

77059646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103361958-T-A

77059646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103361958-T-C

77060366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103362753-G-C

77060443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103362824-T-C

http://identifiers.org/hco/13/GRCh38#77060490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103362875-C-A

http://identifiers.org/hco/13/GRCh38#77060500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103362885-A-C

77060652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103363035-G-A

http://identifiers.org/hco/13/GRCh38#77060742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103363115-C-A

77060742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103363115-C-T

http://identifiers.org/hco/13/GRCh38#77061159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103364048-A-C

77061221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103364110-T-C

77061233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103364122-G-A

77061233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103364122-G-C

77061281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103364170-T-C

http://identifiers.org/hco/13/GRCh38#77061316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103364205-A-C

http://identifiers.org/hco/13/GRCh38#77061321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103364210-C-A

77061321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364210-C-T

77061370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364248-T-A

77061370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364248-T-C

77061416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364293-G-C

77061416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364293-G-T

http://identifiers.org/hco/13/GRCh38#77061429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103364306-C-A

77061429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364306-C-T

77061431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364308-A-G

http://identifiers.org/hco/13/GRCh38#77061454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103364331-C-A

77061531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364407-A-T

http://identifiers.org/hco/13/GRCh38#77061562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103364433-C-A

77061562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364433-C-T

77061601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364458-T-A

77061607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364464-A-G

77061722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103364560-T-C

77061902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364740-G-A

77061902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364740-G-C

77062112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364931-T-C

77062340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103365149-A-G

77062466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103365254-A-G

77062736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103365468-G-A

77062768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103365498-T-C

77062888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103365589-G-C

77063162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103365835-C-T

77063513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366115-G-A

http://identifiers.org/hco/13/GRCh38#77063523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103366125-A-C

77063523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366125-A-G

77063553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366180-T-C

http://identifiers.org/hco/13/GRCh38#77063584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103366215-C-A

77063844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366399-G-T

http://identifiers.org/hco/13/GRCh38#77064138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103366683-A-C

77064275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367073-G-T

http://identifiers.org/hco/13/GRCh38#77064461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103367253-A-C

77064493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367272-T-A

77064493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367272-T-C

77064629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103367381-T-C

77064766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367518-G-T

http://identifiers.org/hco/13/GRCh38#77064783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103367535-C-A

77064783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367535-C-T

77064785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367537-T-C

77064817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367565-T-G

77064829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103367578-T-G

77065205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103368140-T-C

77065472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103368371-A-T

77065620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103368503-T-C

77067453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371127-T-C

77067480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371148-G-A

77067480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371148-G-T

77067613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103371250-T-C

77067688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103371325-T-C

77067688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103371325-T-G

77067700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103371337-G-A

77067811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103371448-G-A

77068456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103371833-G-A

77068456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103371833-G-C

77068456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103371833-G-T

77068495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372406-T-G

77068634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103372539-A-G

77068643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103372548-T-C

77068670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103372575-T-G

http://identifiers.org/hco/13/GRCh38#77068898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103372801-C-A

http://identifiers.org/hco/13/GRCh38#77068967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103372863-C-A

77068978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372872-G-T

77070694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103374058-G-A

77070694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103374058-G-T

77070709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 103374073-T-C

77070709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 103374073-T-G

77070710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 103374074-G-A

77070710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 103374074-G-T

77070715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103374079-T-A

77070715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103374079-T-C

77070715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103374079-T-G

77070814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374181-A-G

77073243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375274-G-A

http://identifiers.org/hco/13/GRCh38#77073487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103375463-A-C

77076205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375656-A-G

77076337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375771-G-T

77076432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375832-G-A

77076537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375923-T-C

77076882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376290-T-C

77076911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376317-G-A

77076911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376317-G-T

77076913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376319-A-G

77076965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376524-A-G

77076971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376530-A-G

77077011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376566-T-C

77077025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376580-G-A

77077025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376580-G-C

77077025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376580-G-T

77077271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103376796-G-A

77077467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376995-G-A

http://identifiers.org/hco/13/GRCh38#77077472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377000-C-A

77077472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377000-C-T

77077485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377010-G-A

http://identifiers.org/hco/13/GRCh38#77077537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377059-C-A

77077537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377059-C-T

http://identifiers.org/hco/13/GRCh38#77077605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377123-C-A

77077605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377123-C-G

77077605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377123-C-T

http://identifiers.org/hco/13/GRCh38#77077612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377130-A-C

77077612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377130-A-G

http://identifiers.org/hco/13/GRCh38#77077621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377139-C-A

77077621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377139-C-G

77077621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377139-C-T

77077685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377202-T-C

77077762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377263-A-T

http://identifiers.org/hco/13/GRCh38#77077916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377472-C-A

http://identifiers.org/hco/13/GRCh38#77077987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377554-C-A

77077987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377554-C-T

http://identifiers.org/hco/13/GRCh38#77078009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377576-C-A

http://identifiers.org/hco/13/GRCh38#77078066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377633-C-A

77078076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377636-A-T

77078286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377832-T-C

77078291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377837-A-T

http://identifiers.org/hco/13/GRCh38#77078318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103377864-A-C

77078359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377905-T-C

77078359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377905-T-G

77078507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378050-G-A

77078518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378061-T-C

77078548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378083-C-T

http://identifiers.org/hco/13/GRCh38#77078549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103378084-C-A

77078549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378084-C-G

http://identifiers.org/hco/13/GRCh38#77078680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103378196-C-A

77078680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378196-C-T

77078725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378239-A-G

77078755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378269-A-G

77078921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378405-C-T

77078993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378476-T-C

77079000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378483-G-A

77079000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378483-G-T

77079009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378488-G-C

77079009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378488-G-T

77079042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378521-G-A

77079058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378537-G-A

77079117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378570-C-T

77079177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378629-G-A

77079289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378716-T-C

77079490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378899-T-C

77080321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379488-G-A

77080388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379542-C-T

http://identifiers.org/hco/13/GRCh38#77080392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103379546-C-A

77080734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379762-G-A

77080734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379762-G-T

http://identifiers.org/hco/13/GRCh38#77080966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103379867-A-C

77080966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379867-A-G

77080974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379875-T-C

77080974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379875-T-G

http://identifiers.org/hco/13/GRCh38#77081021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103379880-C-A

77081021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379880-C-G

77081021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379880-C-T

77081050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379909-T-A

http://identifiers.org/hco/13/GRCh38#77081068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103379933-C-A

77081068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379933-C-G

77081068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379933-C-T

77081072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379937-G-A

77081072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379937-G-C

77081072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103379937-G-T

77081195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380038-T-C

http://identifiers.org/hco/13/GRCh38#77081218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103380061-C-A

77081456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103380209-C-T

77081586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103380339-T-G

77081696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380449-C-T

77081873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103380615-G-A

77081900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103380642-A-G

77082025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103380760-A-G

77082132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103380876-A-T

77082158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103380904-T-C

77082376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381110-T-C

http://identifiers.org/hco/13/GRCh38#77082648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103381358-C-A

77082673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381386-T-G

77082887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381547-T-C

77082912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381570-T-A

77082912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381570-T-C

http://identifiers.org/hco/13/GRCh38#77082949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103381611-C-A

77082949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381611-C-G

77082949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381611-C-T

77082960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381621-G-A

77082960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381621-G-C

77082960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381621-G-T

77083055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103381713-A-G

http://identifiers.org/hco/13/GRCh38#77083145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103381803-A-C

77083541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382112-G-A

77083786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382223-T-A

77084579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382743-C-T

77084610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382767-T-C

77087559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103383411-T-C

77087649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383501-T-A

77087649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383501-T-C

77088142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383634-T-C

77088256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383711-G-A

77088348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383802-C-T

77088355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383809-T-C

77088460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103383929-A-G

http://identifiers.org/hco/13/GRCh38#77088542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103383994-A-C

77088559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384008-T-C

77088630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384071-G-A

77088802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384240-G-A

77088802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384240-G-T

77089067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384502-G-T

77089089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384530-A-G

77089416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103384892-C-G

77089670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385400-A-T

77090020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385724-A-T

77090266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103386104-G-A

77090271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103386109-T-C

77090362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386204-T-A

77090362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386204-T-G

77090418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386286-T-C

77090444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386312-G-A

77090444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386312-G-C

77090444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386312-G-T

http://identifiers.org/hco/13/GRCh38#77090488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103386353-C-A

77090488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386353-C-T

http://identifiers.org/hco/13/GRCh38#77092041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103388232-C-A

77092041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388232-C-T

77092063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388251-G-T

77092066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388254-G-T

77092072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388260-A-T

77092369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388557-T-C

77092423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388607-G-A

77092462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388639-T-C

77092467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103388640-C-T

77092486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388659-G-A

77092489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388662-A-G

77092533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388720-T-C

77092533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388720-T-G

http://identifiers.org/hco/13/GRCh38#77092549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103388736-C-A

77092549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388736-C-T

77092559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388745-G-T

77092569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 103388755-T-C

77092571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388757-T-C

77092575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103388761-T-A

77092581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103388767-T-C

77092915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103389309-C-T

http://identifiers.org/hco/13/GRCh38#77093020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103389402-C-A

77093092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103389493-G-A

77093092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103389493-G-T

77093636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103390002-T-C

77093715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103390082-T-C

http://identifiers.org/hco/13/GRCh38#77093762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103390135-A-C

77094801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103390828-T-C

77095046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103391037-C-T

77095191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103391168-A-G

77095307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103391311-A-G

77095414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103391418-G-A

77095578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103391582-T-C

77096180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392093-G-A

77096180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392093-G-T

77096222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392134-G-T

77096584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392444-G-A

77096584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392444-G-T

77096593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392453-T-A

77097350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103392540-C-T

77097557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103392747-C-T

77097566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103392756-T-C

77097761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103392951-T-C

77097872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393062-T-A

77097872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393062-T-C

77097917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 103393107-C-T

77098037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393227-G-A

77098039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393229-G-A

77098070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393260-G-A

77098070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393260-G-T

http://identifiers.org/hco/13/GRCh38#77098079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103393269-A-C

77098079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393269-A-G

77098196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393386-G-A

77098211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393401-T-C

77098403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393593-T-C

77098403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393593-T-G

http://identifiers.org/hco/13/GRCh38#77098418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103393608-A-C

77098670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393860-T-C

77098703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103393893-A-G

http://identifiers.org/hco/13/GRCh38#77098914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103394104-C-A

77098914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103394104-C-T

77098934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103394124-T-C

77098964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103394154-T-C

77098973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103394163-A-G

77098976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103394166-G-C

http://identifiers.org/hco/13/GRCh38#77099031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103394221-C-A

http://identifiers.org/hco/13/GRCh38#77099074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103394243-C-A

77099074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103394243-C-G

http://identifiers.org/hco/13/GRCh38#77099243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103394391-C-A

http://identifiers.org/hco/13/GRCh38#77099530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103394650-A-C

77099875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103394984-C-T

http://identifiers.org/hco/13/GRCh38#77099882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103394991-C-A

77100004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395114-T-C

77100016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395126-G-T

77100028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395134-A-G

77100048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395149-G-A

77100223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395309-G-A

77100223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395309-G-T

77100311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395384-T-C

77100368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395446-T-C

77101192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103396387-T-C

77101528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103396644-G-C

77101988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103397082-T-G

77102543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103397648-T-A

77102543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103397648-T-C

77102618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103397718-T-C

77102819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103397918-A-T

77102826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103397925-G-A

77103176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103398241-G-A

http://identifiers.org/hco/13/GRCh38#77103259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103398327-C-A

77103883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103398901-A-T

77103919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103398938-T-C

77104200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399164-T-C

77104524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399866-T-A

77105140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400560-C-T

77105184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400626-A-G

77105577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400954-G-T

77105745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401119-G-T

77105747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401121-T-C

77106152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401458-G-A

77106273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401548-T-C

77106324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401598-C-T

77115436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402092-T-A

77115436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402092-T-C

77115524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402198-C-T

77115528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402202-T-A

77115528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402202-T-C

77115528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402202-T-G

77116099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403012-T-G

77116185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403085-C-T

http://identifiers.org/hco/13/GRCh38#77116453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103403312-C-A

77116477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403336-C-G

77116504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403364-G-A

77116504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403364-G-T

77116805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103405602-T-G

77117224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103405934-T-C

77117317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103406093-A-G

77117515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103406352-T-C

77117613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103406503-T-C

77117998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103406861-C-T

77118280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407236-A-T

http://identifiers.org/hco/13/GRCh38#77118303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103407258-A-C

77118396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103407349-A-G

77118543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407495-T-A

77118543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407495-T-C

77119325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408258-T-C

77120800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103409506-T-C

77120944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103409634-T-G

77120948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103409638-G-A

77121111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103409778-C-T

77121139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103409804-A-T

77121474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103410104-T-C

77121593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103410222-G-T

http://identifiers.org/hco/13/GRCh38#77121641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103410256-C-A

77125030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103410899-G-A

77125202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411085-T-A

77125202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411085-T-C

77125676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411557-G-A

77125734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411614-C-T

77125996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411866-C-T

77126002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411872-G-A

77126252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103412139-G-C

77126252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103412139-G-T

77128928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103414465-A-T

77129068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103414603-T-C

77129088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103414622-G-T

77129162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103414698-G-A

http://identifiers.org/hco/13/GRCh38#77129328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103414860-C-A

77129328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103414860-C-G

77129328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103414860-C-T

77129583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103415104-G-T