http://identifiers.org/hco/15/GRCh38#84080200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#82297754-C-A

84080209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 82297763-C-T

http://identifiers.org/hco/15/GRCh38#84080210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#82297764-C-A

84080210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 82297764-C-T

84080256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82297815-G-A

84080256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82297815-G-C

84080256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82297815-G-T

84080266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82297824-A-G

http://identifiers.org/hco/15/GRCh38#84080287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82297844-C-A

84080287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82297844-C-T

http://identifiers.org/hco/15/GRCh38#84080321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82297881-C-A

84080321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82297881-C-T

http://identifiers.org/hco/15/GRCh38#84080325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#82297885-C-A

84080325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 82297885-C-T

84080430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82297950-G-A

84080430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82297950-G-T

http://identifiers.org/hco/15/GRCh38#84080508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82298003-C-A

84080735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298231-G-T

84080866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82298418-C-G

84080942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298488-A-G

84080942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298488-A-T

84081001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298542-T-C

84081025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82298589-T-C

84081025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82298589-T-G

84081043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298606-T-G

http://identifiers.org/hco/15/GRCh38#84081094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#82298679-C-A

84081094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82298679-C-T

http://identifiers.org/hco/15/GRCh38#84081305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82298889-C-A

84081305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298889-C-T

84081311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298895-G-C

84081380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298937-T-A

84081382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82298939-A-T

84081629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82299165-G-A

84081806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82299275-G-A

84081821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82299290-T-C

84082250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82299631-G-A

84082693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82299929-G-A

84082906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82300086-C-T

84083191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82300314-G-A

84083465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82300573-A-G

84083628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82300704-A-G

84083678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82300755-A-G

84083797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82300844-A-T

84084304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82301195-G-A

84084304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82301195-G-T

84084398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82301278-T-C

84084398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82301278-T-G

http://identifiers.org/hco/15/GRCh38#84084542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82301407-A-C

84085521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82302454-A-G

84085644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82302559-G-A

84085778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82302684-G-A

84086051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82302923-G-A

84086065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82302937-G-T

84086217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82303009-A-G

84086268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82303056-A-T

84086273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82303061-G-A

84086945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82305065-A-G

84087370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82305451-A-G

84087564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82305651-A-T

84087643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82305725-A-G

84087729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82305832-A-G

84087821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82305915-G-T

84089093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82306801-C-T

84089312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82306953-G-A

84089386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307013-T-C

84089403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307029-T-C

84090164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307221-T-A

84090164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307221-T-C

84090176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307232-G-T

84090298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307354-G-A

http://identifiers.org/hco/15/GRCh38#84090384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82307440-C-A

84090384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307440-C-G

84090384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307440-C-T

84090443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82307499-G-A

http://identifiers.org/hco/15/GRCh38#84090708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82307803-A-C

84091093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82308153-C-G

84091254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82308294-C-G

84091753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82308789-C-T

84091810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82308844-G-T

84092982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82309481-A-G

http://identifiers.org/hco/15/GRCh38#84093000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82309499-A-C

http://identifiers.org/hco/15/GRCh38#84093012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82309510-C-A

84093175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82309668-T-C

84093387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82309871-G-T

84093506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82309993-A-T

84093567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310046-G-A

84093632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310093-A-G

84093640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310101-C-T

84093786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310461-A-G

84093802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310498-C-T

84093855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310553-C-G

84094314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310780-T-C

84094353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310819-G-C

84094427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82310898-G-T

84094663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82311029-G-A

84095151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82311415-A-G

84095261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82311525-T-A

84095369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82311612-T-C

84095380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82311623-T-C

84095500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82311749-G-C

84095800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82312008-A-G

84096227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313267-G-A

84096363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313405-G-T

84096467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313510-C-G

84096659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313666-T-C

84096783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313783-C-G

84096874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313842-A-G

http://identifiers.org/hco/15/GRCh38#84096900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82313858-A-C

84096984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82313953-T-C

84097035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314006-T-A

84097316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314224-C-T

84097318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314226-T-A

84097353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314265-G-C

http://identifiers.org/hco/15/GRCh38#84098154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82314946-C-A

84098155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314947-C-T

84098162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314954-T-C

84098168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314960-C-T

84098183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82314971-A-G

84098263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82315028-C-T

84098434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82315206-A-G

84098440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82315212-T-G

84098644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82315379-A-G

84098655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82315391-C-T

84099128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316053-A-G

84099250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316185-G-A

84099362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316260-C-T

84099381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316276-G-A

84099382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316277-G-C

84099415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316310-A-G

84099456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316345-G-C

84099529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316386-T-C

84099603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316461-T-C

84099710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316560-A-G

84099718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316568-G-A

84099807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316638-G-C

http://identifiers.org/hco/15/GRCh38#84099812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82316643-A-C

http://identifiers.org/hco/15/GRCh38#84099833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82316661-A-C

84099833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82316661-A-G

84100098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82317095-A-G

84100120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82317107-T-A

84100675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82319553-C-G

84100758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82319617-T-C

84100820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82319674-T-C

84101061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82319783-G-C

84101191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82319903-A-G

84101427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320117-C-T

84101468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320202-G-T

84101631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320485-T-C

84101719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320585-A-G

84101719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320585-A-T

http://identifiers.org/hco/15/GRCh38#84101927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82320718-C-A

84101993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320777-G-A

84101993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320777-G-T

84102033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 82320815-A-G

84102167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320949-A-G

84102188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320969-A-G

84102204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320981-G-A

84102204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320981-G-T

84102214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82320991-A-G

http://identifiers.org/hco/15/GRCh38#84102226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82321005-C-A

84102226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82321005-C-T

http://identifiers.org/hco/15/GRCh38#84102313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82321083-C-A

84102381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82321150-G-T

http://identifiers.org/hco/15/GRCh38#84102730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82321869-C-A

84102737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82321875-G-A

84102737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82321875-G-T

84102931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82322074-T-A

84102931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82322074-T-C

84102979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82322122-G-A

84102979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82322122-G-T

84102994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82322137-T-A

84102994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82322137-T-C

84103039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82322182-A-G

84103122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82322263-G-T

http://identifiers.org/hco/15/GRCh38#84103126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82322267-C-A

http://identifiers.org/hco/15/GRCh38#84103152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82322293-A-C

84103152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82322293-A-T

84103276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82322419-T-C

84103473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82322602-C-T

84104013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323104-T-G

84104472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323456-C-T

http://identifiers.org/hco/15/GRCh38#84104498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82323468-C-A

http://identifiers.org/hco/15/GRCh38#84104520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82323492-C-A

http://identifiers.org/hco/15/GRCh38#84104521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82323493-C-A

http://identifiers.org/hco/15/GRCh38#84104524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82323496-A-C

84104538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323510-G-T

84104539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323511-T-C

http://identifiers.org/hco/15/GRCh38#84104558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82323530-A-C

84104579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323550-C-T

84104844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323810-A-G

84104865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323828-G-A

84104865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323828-G-T

84105045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82323984-A-G

84105082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324016-C-T

84105181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324113-G-A

84105275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324203-T-G

84105534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324660-G-A

84105540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324663-G-T

84105678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324795-G-A

84105769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324877-T-C

http://identifiers.org/hco/15/GRCh38#84105788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82324894-C-A

84105788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324894-C-T

84105813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82324910-A-G

http://identifiers.org/hco/15/GRCh38#84108677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82325876-C-A

http://identifiers.org/hco/15/GRCh38#84109156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82326450-A-C

84111437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82331307-T-A

84111437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82331307-T-C

http://identifiers.org/hco/15/GRCh38#84111548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82331414-C-A

84111548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82331414-C-T

http://identifiers.org/hco/15/GRCh38#84111877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82332082-A-C

84112210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82332368-T-C

84112235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82332393-A-G

84112246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82332410-A-T

84112389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82332542-G-A

84113004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333082-G-A

84113004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333082-G-T

http://identifiers.org/hco/15/GRCh38#84113073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82333156-C-A

84113080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333163-A-G

84113084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333167-T-A

84113084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333167-T-C

84113140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333224-T-A

84113220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333285-T-C

84113378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333343-G-C

84113466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333433-T-C

84113472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333439-A-G

84113472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333439-A-T

84113499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333465-T-A

84113499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333465-T-C

84113544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333490-G-A

84113544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82333490-G-T

84113616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82333558-T-G

http://identifiers.org/hco/15/GRCh38#84113628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82333570-C-A

84113628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82333570-C-T

84113647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82333589-A-G

84113647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82333589-A-T

84113694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82333636-A-G

84113961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334047-C-G

84113988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334073-C-T

http://identifiers.org/hco/15/GRCh38#84114072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82334161-C-A

84114086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334175-C-T

84114137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334213-C-G

84114190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334265-A-T

84114379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334376-T-C

http://identifiers.org/hco/15/GRCh38#84114569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82334576-A-C

http://identifiers.org/hco/15/GRCh38#84114601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82334592-C-A

84114615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334605-T-C

84114633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334623-A-T

84114761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334747-A-G

84114784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334768-C-T

84114799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334783-A-G

84115654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82335410-C-T

84115842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82335694-C-G

84116086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82335914-A-G

84116086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82335914-A-T

84116210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336047-G-A

84116340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336166-G-A

84116437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336255-C-T

84116565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336366-A-G

84116598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336391-C-G

84117459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336717-T-A

84117739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82336956-T-C

84117886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337084-T-A

84117914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337115-G-T

84117949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337183-C-T

84118088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337321-A-T

84118099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337332-A-G

84118133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337367-G-T

84118216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82337450-C-T

84118483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82338784-G-A

84118502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82338802-A-G

84118554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82338836-G-A

84118617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82338895-T-C

84118843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339622-T-C

http://identifiers.org/hco/15/GRCh38#84118980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82339737-A-C

84118980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339737-A-G

84119002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339755-A-G

84119111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339866-A-G

84119117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339872-G-A

84119146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339901-A-G

http://identifiers.org/hco/15/GRCh38#84119220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82339949-C-A

84119255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82339994-A-G

http://identifiers.org/hco/15/GRCh38#84119485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82340426-A-C

84119495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82340436-A-G

84119868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82340643-A-G

84120233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82340973-A-T

http://identifiers.org/hco/15/GRCh38#84120285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82341024-A-C

84120308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341055-C-T

84120651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341239-T-G

84120844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341417-G-A

84120844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341417-G-T

http://identifiers.org/hco/15/GRCh38#84120846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82341419-C-A

http://identifiers.org/hco/15/GRCh38#84120987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82341548-C-A

84120987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341548-C-G

http://identifiers.org/hco/15/GRCh38#84120998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82341558-C-A

84120998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341558-C-T

84121038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341591-C-G

84121038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341591-C-T

84121220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82341801-C-G

84121283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341864-T-A

84121299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341880-G-A

http://identifiers.org/hco/15/GRCh38#84121301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82341882-C-A

84121301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82341882-C-T

84121696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342231-A-G

84121716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342249-G-T

84121762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342278-G-A

84121781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342289-A-G

http://identifiers.org/hco/15/GRCh38#84121789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82342297-C-A

84121789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342297-C-G

84121789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342297-C-T

http://identifiers.org/hco/15/GRCh38#84121849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82342359-A-C

84122103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342564-A-T

http://identifiers.org/hco/15/GRCh38#84122348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82342727-C-A

84122348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342727-C-T

http://identifiers.org/hco/15/GRCh38#84122378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82342756-C-A

84122389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342767-G-A

84122389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342767-G-T

84122446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342819-G-A

84122450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342823-G-A

84122462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342833-G-A

84122556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82342893-C-T

84122975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82343244-A-G

84122994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82343266-A-T

84124121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82344884-T-C

84124125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82344888-C-T

84124181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82344940-T-C

84124536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82345239-A-G

84124601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82345306-T-G

84124654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82345377-T-C

84124780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82345504-G-T

84124830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82345565-G-A

84124830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82345565-G-T

84125674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346344-A-G

84125722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346389-A-G

http://identifiers.org/hco/15/GRCh38#84125774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82346401-C-A

84125806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346435-T-C

84125834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346462-G-A

84125884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346507-G-A

84125994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346599-A-G

84125994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346599-A-T

84126005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346610-A-G

84126005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346610-A-T

84126330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346939-A-T

http://identifiers.org/hco/15/GRCh38#84126368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#82346976-C-A

84126368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82346976-C-T

84126575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31739
most severe consequence: non coding transcript exon variant
orthologous variants: 82347200-G-A