133453932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non coding transcript exon variant
orthologous variants: 139798430-T-A

133454023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139798503-G-A

133454089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798572-T-G

http://identifiers.org/hco/10/GRCh38#133454094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139798577-C-A

133454129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798611-C-T

133454142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798624-G-A

133454142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798624-G-C

133454208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798681-G-A

133454245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798728-G-T

133454537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139798996-G-A

133454619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799046-C-G

133454619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799046-C-T

133454673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799091-C-T

133454701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799112-C-T

133455543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799717-A-G

133455612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799748-T-C

133455713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799843-G-A

133455723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139799853-G-T

133455936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800040-T-C

133456118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800211-T-C

133456123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800216-G-A

133456156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800234-G-A

http://identifiers.org/hco/10/GRCh38#133456191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139800256-C-A

133456191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800256-C-T

http://identifiers.org/hco/10/GRCh38#133456584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139800628-C-A

133456584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800628-C-T

133456618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800666-G-A

133456618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800666-G-T

133456631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800679-G-A

133456631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800679-G-C

133456631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139800679-G-T

http://identifiers.org/hco/10/GRCh38#133456937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139800991-C-A

133457032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139801061-C-G

133457032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139801061-C-T

133457060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139801089-G-A

133457060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139801089-G-C

133457060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139801089-G-T

133457078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139801104-G-T

133457416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139802207-G-C

133457457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139802248-C-T

http://identifiers.org/hco/10/GRCh38#133457649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139802424-A-C

133457649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802424-A-G

133457649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802424-A-T

http://identifiers.org/hco/10/GRCh38#133457660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139802439-C-A

133457660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802439-C-T

133457684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802522-T-C

http://identifiers.org/hco/10/GRCh38#133457773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139802612-C-A

133457773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802612-C-T

http://identifiers.org/hco/10/GRCh38#133457836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139802666-C-A

133457864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802694-T-C

133457920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802750-T-G

133457926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802759-T-C

http://identifiers.org/hco/10/GRCh38#133458029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139802839-C-A

http://identifiers.org/hco/10/GRCh38#133458083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139802882-C-A

133458083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802882-C-G

133458083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802882-C-T

133458105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802904-G-T

133458177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802962-C-T

133458213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139802985-G-C

133458285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139803052-C-T

133458324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139803091-C-T

133458364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139803133-C-T

133458446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139803227-C-T

133458564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139803345-G-A

133458610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139803391-T-C

133458648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139803429-G-A

133458684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803462-G-A

133458684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803462-G-T

http://identifiers.org/hco/10/GRCh38#133458740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139803535-C-A

133458740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803535-C-T

133458778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803576-G-A

133458877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803671-G-A

133458877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803671-G-T

133458880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803674-G-T

133458882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803676-A-G

133458933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803715-C-T

133458983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803762-G-A

133458986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803765-G-A

133458986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803765-G-T

http://identifiers.org/hco/10/GRCh38#133459012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139803795-C-A

133459012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139803795-C-T

http://identifiers.org/hco/10/GRCh38#133459044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139803827-A-C

133459044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139803827-A-G

133459094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139803877-C-T

133459116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139803899-A-G

133459169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139803952-C-T

http://identifiers.org/hco/10/GRCh38#133459207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139803990-C-A

133459207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139803990-C-T

133459221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804004-G-A

133459221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804004-G-T

133459286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804069-G-A

133459286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804069-G-T

http://identifiers.org/hco/10/GRCh38#133459350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804124-C-A

133459350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139804124-C-T

133459539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804285-C-T

133459573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804319-G-A

http://identifiers.org/hco/10/GRCh38#133459576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804322-C-A

133459576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804322-C-T

133459582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804328-G-A

133459582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804328-G-C

133459582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804328-G-T

http://identifiers.org/hco/10/GRCh38#133459599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804345-C-A

133459599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804345-C-G

133459599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804345-C-T

http://identifiers.org/hco/10/GRCh38#133459645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804391-C-A

133459645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139804391-C-T

http://identifiers.org/hco/10/GRCh38#133459698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804444-C-A

http://identifiers.org/hco/10/GRCh38#133459751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804497-C-A

133459751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804497-C-T

http://identifiers.org/hco/10/GRCh38#133459837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804582-C-A

133459837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139804582-C-T

http://identifiers.org/hco/10/GRCh38#133459848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139804593-C-A

133459962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804729-G-A

133459962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804729-G-T

133460070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804837-G-A

133460088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139804855-G-A

133460088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139804855-G-T

133464448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807565-T-A

133464448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807565-T-G

133464489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807603-T-C

133464499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807661-A-G

133464573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807746-G-A

133464591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807755-G-A

133464591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807755-G-C

133464591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807755-G-T

133464610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139807774-G-A

133464610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139807774-G-C

133464647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807811-G-A

133464647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139807811-G-T

http://identifiers.org/hco/10/GRCh38#133464656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139807820-C-A

133464656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139807820-C-T

133464715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139807879-C-G

133464956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808113-G-A

133464956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808113-G-T

133465016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808175-G-C

133465037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808189-G-A

133465037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808189-G-C

133465087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808238-G-T

133465093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139808244-G-C

http://identifiers.org/hco/10/GRCh38#133465315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139808481-C-A

133465315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139808481-C-T

133465465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139808631-G-A

133465549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139808715-G-A

133465564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139808730-G-T

133473639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899637-C-G

133473639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899637-C-T

133473730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899726-T-G

133473774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899763-T-C

133473827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899816-T-C

133473929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899916-A-G

133473932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139899919-G-T

133474045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900015-G-T

133474070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900039-C-T

133474218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900117-C-G

133474284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900150-C-T

133474395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900215-A-G

133474408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900231-T-C

133474421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900244-C-T

133474427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900250-G-A

133474475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900263-G-C

133474475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900263-G-T

133474530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900273-T-C

http://identifiers.org/hco/10/GRCh38#133474553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139900284-A-C

133474555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900286-G-A

133474556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900287-C-T

http://identifiers.org/hco/10/GRCh38#133474784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139900388-A-C

133474830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900421-G-A

http://identifiers.org/hco/10/GRCh38#133474888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139900477-C-A

133474888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900477-C-T

http://identifiers.org/hco/10/GRCh38#133474893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139900482-A-C

133474906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900496-C-T

133474928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900523-C-T

133475062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900661-G-A

133475175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900753-G-A

133475248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900817-T-C

133475253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900822-C-T

133475280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900849-C-G

133475280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900849-C-T

133475292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900862-C-T

133475295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900864-C-T

133475302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900871-C-G

133475312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900881-C-T

133475325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900893-G-A

133475325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139900893-G-C

133475477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901134-G-A

133475483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901140-C-T

133475520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901178-C-T

133475625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901269-T-C

133475717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901363-G-A

133476032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901695-T-C

133476077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139901748-G-A

133476332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902033-T-C

133481184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902579-G-A

133481206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902600-G-A

http://identifiers.org/hco/10/GRCh38#133481209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902603-C-A

http://identifiers.org/hco/10/GRCh38#133481211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902605-C-A

133481211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902605-C-G

133481211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902605-C-T

133481215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902609-C-G

133481230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902623-G-A

133481230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902623-G-C

133481230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139902623-G-T

http://identifiers.org/hco/10/GRCh38#133481243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902637-C-A

133481243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902637-C-T

133481256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902650-G-A

133481256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902650-G-T

133481264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902658-G-A

133481264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902658-G-C

133481264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902658-G-T

http://identifiers.org/hco/10/GRCh38#133481283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902677-C-A

http://identifiers.org/hco/10/GRCh38#133481288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902682-C-A

133481288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902682-C-G

133481288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902682-C-T

133481292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902686-G-T

http://identifiers.org/hco/10/GRCh38#133481315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902712-C-A

http://identifiers.org/hco/10/GRCh38#133481345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902742-C-A

133481353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902750-T-A

133481361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902758-A-G

133481363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902760-C-T

133481373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902770-C-G

http://identifiers.org/hco/10/GRCh38#133481374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902771-C-A

133481374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902771-C-T

133481377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902774-G-T

133481390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902787-A-G

133481390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902787-A-T

http://identifiers.org/hco/10/GRCh38#133481396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902793-C-A

133481396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902793-C-T

133481402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902799-T-C

http://identifiers.org/hco/10/GRCh38#133481429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139902826-C-A

133481429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902826-C-G

133481429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902826-C-T

133481430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902827-G-A

133481430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139902827-G-T

http://identifiers.org/hco/10/GRCh38#133481450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903423-C-A

133481450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903423-C-G

133481450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903423-C-T

133481451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903424-A-G

133481459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903432-G-T

133481465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903438-T-A

133481465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903438-T-C

133481471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903444-G-A

133481471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903444-G-T

http://identifiers.org/hco/10/GRCh38#133481488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903461-C-A

133481488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903461-C-T

http://identifiers.org/hco/10/GRCh38#133481492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903465-C-A

133481492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903465-C-T

http://identifiers.org/hco/10/GRCh38#133481499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903472-C-A

http://identifiers.org/hco/10/GRCh38#133481501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903475-C-A

133481501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903475-C-T

133481502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903476-T-C

133481533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903507-A-G

133481536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903510-A-G

133481564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903538-A-T

133481566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903540-G-A

133481582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903556-T-A

133481584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903558-T-C

133481588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903562-G-C

133481597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903571-G-A

133481597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903571-G-T

http://identifiers.org/hco/10/GRCh38#133481600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903574-C-A

133481600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903574-C-G

http://identifiers.org/hco/10/GRCh38#133481601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903575-C-A

133481606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903580-G-T

133481617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903591-A-G

133481638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139903610-G-T

133481956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903707-G-C

133481959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903710-A-G

133481972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903723-C-T

133481978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903729-T-C

133481978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903729-T-G

133482024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903767-G-A

133482081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903812-C-T

133482082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903813-G-A

http://identifiers.org/hco/10/GRCh38#133482123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139903841-A-C

133482167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139903876-G-A