7758882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36161038-T-G

7758914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36161002-C-T

7759139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36160727-T-G

7759196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36160683-T-C

7759345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36160565-G-T

7759411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36160519-G-C

7760249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36160007-G-A

7760249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36160007-G-T

7760296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159964-G-A

7760312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159948-G-C

7760313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159947-G-A

7760338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159924-G-A

7760338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159924-G-T

http://identifiers.org/hco/4/GRCh38#7761326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36159071-C-A

7761326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159071-C-T

7761332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36159067-C-T

7761436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158980-G-A

7761436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158980-G-T

http://identifiers.org/hco/4/GRCh38#7761549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36158938-C-A

7761549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158938-C-T

7761842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158716-G-T

7761868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158699-G-A

7761868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158699-G-T

7761879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158694-G-A

7761879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158694-G-C

7761879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158694-G-T

http://identifiers.org/hco/4/GRCh38#7761889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36158684-C-A

7761889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158684-C-T

7761930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158635-C-T

7761941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158624-G-A

7761941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158624-G-C

7761941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36158624-G-T

7761988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158584-G-C

7762120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158477-G-T

7762223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158386-G-C

7762223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158386-G-T

7762234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158375-G-A

7762234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158375-G-C

7762234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158375-G-T

7762284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158347-T-C

7762315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158317-G-T

7762329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158307-G-T

http://identifiers.org/hco/4/GRCh38#7762458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36158209-C-A

7762484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158180-G-A

7762484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158180-G-C

7762485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158179-C-T

http://identifiers.org/hco/4/GRCh38#7762586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36158093-C-A

http://identifiers.org/hco/4/GRCh38#7762677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36158012-C-A

7762677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158012-C-G

7762677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158012-C-T

http://identifiers.org/hco/4/GRCh38#7762680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36158009-C-A

7762680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36158009-C-T

7762740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157974-A-G

7762833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157900-G-A

7762833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157900-G-T

7762899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157867-G-T

http://identifiers.org/hco/4/GRCh38#7762915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36157851-C-A

7762915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157851-C-T

7762929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157845-G-A

7762929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157845-G-T

7763094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157649-C-T

7763246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157495-G-C

7763246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157495-G-T

7763325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157430-G-A

7763325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157430-G-C

7763325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157430-G-T

http://identifiers.org/hco/4/GRCh38#7763335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36157420-A-C

7763335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157420-A-T

http://identifiers.org/hco/4/GRCh38#7763342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36157413-C-A

7763342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157413-C-T

http://identifiers.org/hco/4/GRCh38#7763359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36157401-C-A

7763359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157401-C-T

http://identifiers.org/hco/4/GRCh38#7763424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36157368-C-A

7763424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157368-C-G

7763424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157368-C-T

7763425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157367-T-A

7763444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157348-G-C

7763444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157348-G-T

7763456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157336-G-A

7763456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157336-G-C

7763456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157336-G-T

7763655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157157-T-C

7763655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36157157-T-G

7768230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155491-C-G

7768301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155421-T-C

7768525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155235-C-T

http://identifiers.org/hco/4/GRCh38#7768526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36155234-C-A

7768526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155234-C-T

7768614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155160-T-C

7768663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155127-C-T

7768697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155100-A-G

7768697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36155100-A-T

7769053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154817-C-T

7769059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154811-T-C

7769141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154735-A-G

7769470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154532-G-T

7769619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154382-C-T

http://identifiers.org/hco/4/GRCh38#7769656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36154351-A-C

7769656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154351-A-G

7769656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154351-A-T

7769732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154306-G-A

7769732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154306-G-C

7769742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154304-T-C

7769778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154272-T-C

7770045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36154045-C-T

7770163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36153960-G-A

7772908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36153401-T-C

7772938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36153371-T-C

7773016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36153293-A-G

http://identifiers.org/hco/4/GRCh38#7773466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36152158-A-C

http://identifiers.org/hco/4/GRCh38#7773475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36152146-C-A

7773561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36152049-T-C

http://identifiers.org/hco/4/GRCh38#7773574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36152041-C-A

7773616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36152024-G-C

7773616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36152024-G-T

http://identifiers.org/hco/4/GRCh38#7773620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36152020-A-C

7773670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151985-C-T

7773736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151922-C-T

http://identifiers.org/hco/4/GRCh38#7773756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36151900-C-A

7773756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151900-C-T

7773778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151882-C-G

7773780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151880-T-C

7773843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151819-T-A

7773843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151819-T-C

7773843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151819-T-G

7773855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151806-G-A

7773855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151806-G-C

7773855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151806-G-T

7773946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151726-G-A

7773946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151726-G-C

7773946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151726-G-T

http://identifiers.org/hco/4/GRCh38#7773954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36151718-C-A

7773954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151718-C-G

7773954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151718-C-T

http://identifiers.org/hco/4/GRCh38#7773985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36151692-C-A

7773985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151692-C-G

7773985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151692-C-T

7774166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151523-A-G

7774169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151520-C-G

7774241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151462-C-T

http://identifiers.org/hco/4/GRCh38#7774283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36151422-C-A

7774283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151422-C-T

7774294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151413-A-G

7774453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151288-A-G

7774481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151265-G-A

7774481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151265-G-T

7774545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151213-G-A

7774545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151213-G-T

http://identifiers.org/hco/4/GRCh38#7774551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36151206-C-A

7774551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151206-C-G

7774551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151206-C-T

http://identifiers.org/hco/4/GRCh38#7774689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36151097-A-C

7774699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36151088-A-G

7774804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36150982-C-T

7774909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36150877-G-A

7775374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36150686-G-C

7776817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148729-A-G

7776888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148665-C-T

7777045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148509-G-A

7777102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148455-G-A

7777102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148455-G-T

7777109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148448-A-G

http://identifiers.org/hco/4/GRCh38#7777110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36148447-C-A

7777269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148293-G-T

7777358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148220-G-A

7777358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148220-G-C

7777358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148220-G-T

http://identifiers.org/hco/4/GRCh38#7777538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36148067-C-A

7777538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148067-C-T

7777554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148051-A-G

7777594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148015-G-A

7777594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148015-G-C

7777594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36148015-G-T

http://identifiers.org/hco/4/GRCh38#7777620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147997-C-A

7777620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147997-C-T

7777655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147962-T-A

7777668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147950-G-C

7777668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147950-G-T

http://identifiers.org/hco/4/GRCh38#7777774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147885-A-C

7777774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147885-A-G

http://identifiers.org/hco/4/GRCh38#7777802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147856-C-A

7777856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147810-T-C

http://identifiers.org/hco/4/GRCh38#7777865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147801-C-A

http://identifiers.org/hco/4/GRCh38#7778023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147638-C-A

http://identifiers.org/hco/4/GRCh38#7778097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147581-C-A

7778097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147581-C-T

7778112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147566-G-A

7778112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147566-G-T

7778114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147564-T-C

7778114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147564-T-G

7778118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147560-C-G

7778118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147560-C-T

7778126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147552-G-C

7778162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147518-T-C

7778183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147497-G-A

7778183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147497-G-T

http://identifiers.org/hco/4/GRCh38#7778193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147490-A-C

http://identifiers.org/hco/4/GRCh38#7778265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147419-C-A

7778265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147419-C-G

7778265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147419-C-T

7778358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147330-G-A

7778358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147330-G-C

7778358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147330-G-T

7778367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147321-G-A

7778367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147321-G-C

7778367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147321-G-T

7778384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36147302-A-G

http://identifiers.org/hco/4/GRCh38#7778409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147277-C-A

7778409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147277-C-T

7778508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147222-T-C

7778519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147211-A-T

http://identifiers.org/hco/4/GRCh38#7778583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147178-A-C

7778613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147156-T-A

7778613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147156-T-C

7778613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147156-T-G

7778626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147144-G-A

7778626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147144-G-T

http://identifiers.org/hco/4/GRCh38#7778647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36147122-C-A

7778672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147096-C-G

7778672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147096-C-T

7778679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147089-T-C

7778708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147060-G-T

7778730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36147040-C-T

7778852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36146920-C-T

7778857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36146915-G-A

7778857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36146915-G-C

http://identifiers.org/hco/4/GRCh38#7778901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36146874-A-C

7778901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146874-A-G

7778901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146874-A-T

7778919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146864-G-A

7778919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146864-G-C

7778919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146864-G-T

7778991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146791-T-C

7778995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146787-T-A

7778995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146787-T-C

7778995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146787-T-G

http://identifiers.org/hco/4/GRCh38#7779071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36146723-A-C

7779077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146714-G-A

7779077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146714-G-C

7779077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146714-G-T

7779079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146712-T-G

http://identifiers.org/hco/4/GRCh38#7779120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36146664-C-A

7779120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36146664-C-T

7779213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36146552-T-A

7779213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36146552-T-C

7779213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36146552-T-G

7779270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36146496-G-T

7779332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36146447-G-C

7779332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36146447-G-T

7779613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145994-C-G

7779842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145763-C-T

7780339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145346-G-A

7780347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145338-T-A

7780365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145320-T-C

7780366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145319-C-T

7780392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145287-A-G

7780497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36145181-G-A

7781130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144812-T-C

7781304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144717-A-G

7781314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144711-A-T

7781594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36144430-T-A

7781667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36144364-A-G

http://identifiers.org/hco/4/GRCh38#7781676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36144355-C-A

http://identifiers.org/hco/4/GRCh38#7781809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36144284-C-A

7781838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144265-C-T

7781965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144145-G-A

7782101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144028-T-C

7782128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36144012-C-T

7782166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143978-C-T

7782177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143967-A-G

7782234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143912-G-T

7782242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143904-C-T

7782297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143838-G-C

7782575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143398-T-C

7782631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143343-G-C

7782631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143343-G-T

7782694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143282-C-T

7782894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143073-G-C

7782937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36143045-G-C

7782988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36142994-T-C

7783594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36142693-A-G

http://identifiers.org/hco/4/GRCh38#7786167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36141673-C-A

7786167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36141673-C-G

7786167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36141673-C-T

http://identifiers.org/hco/4/GRCh38#7786344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36141511-C-A

7786344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36141511-C-G

7786344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36141511-C-T

http://identifiers.org/hco/4/GRCh38#7786363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36141502-A-C

http://identifiers.org/hco/4/GRCh38#7786421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36141449-A-C

7786421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36141449-A-G

7790017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36138501-T-C

7790159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36138359-A-G

7790211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36138309-C-G

7790521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36137987-C-T

http://identifiers.org/hco/4/GRCh38#7793007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36134596-A-C

7793120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134487-A-G

7793151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134459-A-T

7793297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134315-C-T

7793302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134310-T-A

7793486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134165-G-A

http://identifiers.org/hco/4/GRCh38#7793501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36134150-A-C

7793519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134132-G-A

7793640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134020-T-C

7793660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36134003-T-C

7793693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36133967-T-A

7793693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36133967-T-C

7793729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36133931-T-C

7793741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36133919-T-C

7793747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36133913-A-G

7793759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36133901-T-C

http://identifiers.org/hco/4/GRCh38#7793771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36133889-C-A

7793842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36133820-A-G

7793848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36133814-T-C

7793848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36133814-T-G

7800311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36132058-A-T

7800329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36132041-G-A

7800329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36132041-G-T

7800382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131993-T-C

7800382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131993-T-G

7800398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131984-G-A

7800398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131984-G-T

http://identifiers.org/hco/4/GRCh38#7800431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36131951-A-C

http://identifiers.org/hco/4/GRCh38#7800464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36131919-C-A

7800464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36131919-C-T

7800487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36131896-C-G

7800488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36131895-A-G

7800753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131656-G-A

7800753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131656-G-C

7800753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131656-G-T

7800998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131451-G-C

7801064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131384-A-G

7801076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131372-T-G

7801163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131313-T-C

7801185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36131292-C-T

7803145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36130321-G-A

7803765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129684-A-T

7803882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129565-A-G

7803883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129564-T-C

7803988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129487-G-A

7804025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129452-G-A

7804027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129450-G-A

7804085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129423-T-A

7804085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36129423-T-G

http://identifiers.org/hco/4/GRCh38#7804219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36129371-C-A

7804254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36129352-C-G

http://identifiers.org/hco/4/GRCh38#7806040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36128662-A-C

7806195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36128508-G-A

7806486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36128318-T-C

http://identifiers.org/hco/4/GRCh38#7806883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36127984-C-A

http://identifiers.org/hco/4/GRCh38#7807193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36127689-C-A

7807237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127632-T-C

7807320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127520-T-C

7807325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127515-A-G

7807422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127410-T-A

7807577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127269-A-G

7807586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127261-C-T

7807632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36127218-A-G

7807651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36127200-C-G

7807652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36127199-T-C

7807652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36127199-T-G

7808278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36126670-A-G

7808328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36126625-G-A

7808328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36126625-G-C

7808464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36126489-T-C

7808465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36126488-G-T

7809625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36126050-A-T

7809793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125894-T-C

7809810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125877-T-C

7809810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125877-T-G

7809829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125868-T-A

7809836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125861-A-G

http://identifiers.org/hco/4/GRCh38#7809838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36125859-A-C

http://identifiers.org/hco/4/GRCh38#7809995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36125766-A-C

7810280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125624-G-T

7810338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125561-A-G

7810406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125502-A-G

7810649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125250-T-A

http://identifiers.org/hco/4/GRCh38#7810683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36125217-C-A

7810699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125201-G-A

7810707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125193-T-C

7810764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125151-G-C

7810764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36125151-G-T

7811030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36124894-C-T

7811115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36124814-G-A

7811293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36124660-A-G

http://identifiers.org/hco/4/GRCh38#7811386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36124579-A-C

7811396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36124572-C-T

7811482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36124501-G-A

http://identifiers.org/hco/4/GRCh38#7811483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36124500-C-A

7811500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36124483-G-A

http://identifiers.org/hco/4/GRCh38#7811941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36123214-C-A

7812030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36123134-G-T

7812235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36122919-G-A

7813241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36122108-G-A

7813282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36122070-G-C

http://identifiers.org/hco/4/GRCh38#7813351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36122012-A-C

http://identifiers.org/hco/4/GRCh38#7813393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36121971-C-A

http://identifiers.org/hco/4/GRCh38#7814068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36121035-C-A

7814068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36121035-C-G

7814159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120949-C-T

7814233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120880-G-C

7814318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120843-C-G

7814465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120702-C-T

http://identifiers.org/hco/4/GRCh38#7814755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36120487-C-A

7814755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120487-C-T

7814903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120346-T-C

7814987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120264-C-T

7815170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36120085-G-A

http://identifiers.org/hco/4/GRCh38#7815193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36120062-C-A

7815382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119876-G-A

http://identifiers.org/hco/4/GRCh38#7815900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36119723-C-A

7815900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119723-C-T

http://identifiers.org/hco/4/GRCh38#7815931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36119695-C-A

7815931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119695-C-G

7815931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119695-C-T

http://identifiers.org/hco/4/GRCh38#7815944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36119682-C-A

7815944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119682-C-G

7815944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119682-C-T

7815945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119681-A-G

7815945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119681-A-T

7815954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119672-T-C

7815954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119672-T-G

7815968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119661-T-G

7816001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119647-G-A

7816001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119647-G-T

7816002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119646-C-T

7816035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36119611-C-T

7816155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119491-G-C

7816155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119491-G-T

7816157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119489-G-A

7816157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119489-G-T

7816158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36119488-T-C

7819097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: synonymous variant
orthologous variants: 36119168-C-G

7819097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: synonymous variant
orthologous variants: 36119168-C-T

http://identifiers.org/hco/4/GRCh38#7819283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36118975-C-A

http://identifiers.org/hco/4/GRCh38#7819287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36118970-A-C

7823584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115886-C-G

7823608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115866-G-A

7823608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115866-G-C

7823623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115851-C-G

7823638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115834-C-G

7823638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115834-C-T

7823639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115833-T-C

http://identifiers.org/hco/4/GRCh38#7823830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36115668-C-A

7823831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115667-C-G

7823831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115667-C-T

7823938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115578-G-A

7824234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115360-G-A

7824234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115360-G-T

http://identifiers.org/hco/4/GRCh38#7824248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36115346-A-C

7824367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115235-T-C

7824390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115212-C-T

7824477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115107-G-A

7824571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36115009-A-G

7824598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36114985-G-A

7825898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-C

7825971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-A

7825971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-C

7826011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -A-G

7826052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -T-C

7826132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-T

7826166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/4/GRCh38#7826215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -C-A

7826260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -T-C

7826393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -C-T

7826396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -C-T

7826422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-A

7826422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-C

7826422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-T

7826584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -C-T

7826623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -C-T

7826741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -G-A

http://identifiers.org/hco/4/GRCh38#7827019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -A-C

7827127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: -A-G

7831655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111492-G-A

7831655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111492-G-C

7831709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111456-A-G

7831742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111425-T-C

http://identifiers.org/hco/4/GRCh38#7831850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36111324-C-A

7831850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111324-C-T

7831852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111322-C-T

http://identifiers.org/hco/4/GRCh38#7831873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36111305-C-A

7831910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111202-A-T

7831958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111121-T-C

7831958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111121-T-G

7831999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111082-C-G

7832032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36111049-C-T

7837065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36109523-T-A

http://identifiers.org/hco/4/GRCh38#7837098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36109487-C-A

7837098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36109487-C-T

7837129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36109443-T-C

http://identifiers.org/hco/4/GRCh38#7837400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36109246-C-A

7837463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36109214-C-T

7837554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36109125-T-G

7837659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36109028-G-T

7837721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36108969-A-G

7838396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36108474-G-A

7838396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36108474-G-T

7838546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36108354-T-C

7838740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36108160-G-A

7839447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36107908-T-C

7841754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36106887-T-G

http://identifiers.org/hco/4/GRCh38#7841906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36106767-A-C

7842212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36106470-G-C

7842525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36106136-G-A

7842539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36106124-G-A

http://identifiers.org/hco/4/GRCh38#7842615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36106063-A-C

7842615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36106063-A-G

7842615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36106063-A-T

7842669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36106010-G-T

http://identifiers.org/hco/4/GRCh38#7842670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36106009-C-A

7842670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36106009-C-T

7842696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105983-A-G

http://identifiers.org/hco/4/GRCh38#7842871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105774-A-C

7842871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105774-A-G

7842871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105774-A-T

7842873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105772-G-A

7842873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105772-G-T

http://identifiers.org/hco/4/GRCh38#7842875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105770-C-A

7842875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105770-C-T

http://identifiers.org/hco/4/GRCh38#7842876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105769-C-A

7842876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105769-C-T

7842877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105768-T-C

7842878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105767-G-C

7842878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36105767-G-T

http://identifiers.org/hco/4/GRCh38#7843007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105695-C-A

7843007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36105695-C-T

7843020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36105686-G-A

7843020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36105686-G-T

http://identifiers.org/hco/4/GRCh38#7843024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105682-A-C

7843024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36105682-A-G

http://identifiers.org/hco/4/GRCh38#7843044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105669-C-A

7843044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36105669-C-T

http://identifiers.org/hco/4/GRCh38#7843090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105628-C-A

7843108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36105620-C-T

http://identifiers.org/hco/4/GRCh38#7843242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105485-A-C

7843242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36105485-A-G

7843290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36105437-C-G

http://identifiers.org/hco/4/GRCh38#7843392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105341-C-A

http://identifiers.org/hco/4/GRCh38#7843425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105321-C-A

7843533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36105239-A-G

http://identifiers.org/hco/4/GRCh38#7843675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105117-A-C

7843675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36105117-A-G

http://identifiers.org/hco/4/GRCh38#7843691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36105103-C-A

7843691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36105103-C-T

7843699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36105095-A-G

7843699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36105095-A-T

7843816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36104988-A-G

7843927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104882-G-T

7843933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104876-T-C

7843985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104838-G-A

7843985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104838-G-T

7844054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104790-G-A

7844168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104694-T-C

http://identifiers.org/hco/4/GRCh38#7844180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36104687-C-A

7844239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36104631-T-C

7844318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36104557-G-A

http://identifiers.org/hco/4/GRCh38#7844437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36104441-C-A

7844437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36104441-C-T

7844559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104319-A-G

7845585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104075-G-A

7845613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36104050-G-A

7845720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103973-C-G

7845728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103963-A-G

7845729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103962-C-T

7845884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103788-G-A

7845884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103788-G-T

7845885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103787-G-A

7845885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103787-G-C

7845885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103787-G-T

7845927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103755-T-C

7845963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103723-G-A

7845971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103715-G-A

http://identifiers.org/hco/4/GRCh38#7845984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36103710-A-C

7846007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103694-C-T

7846072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36103635-A-G

http://identifiers.org/hco/4/GRCh38#7855131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36102968-A-C

7855175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102929-C-T

http://identifiers.org/hco/4/GRCh38#7855239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36102874-C-A

7855239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102874-C-T

7855274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102823-G-A

7855280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102817-T-C

7855321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102782-C-G

7855321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102782-C-T

7855323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102780-G-T

7855335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102767-G-A

7855335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102767-G-T

http://identifiers.org/hco/4/GRCh38#7855356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36102746-C-A

7855421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102681-T-C

7855442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102660-G-A

7855442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102660-G-C

7855543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36102561-G-A

7855598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102506-A-G

7855869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102308-C-G

7855890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102287-T-C

7855908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102270-G-A

7855912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36102256-T-C

7856274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101917-G-T

7856303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36101909-C-T

7856442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101782-C-T

7856536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101708-G-T

7856587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101676-T-A

7856587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101676-T-G

7856638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101640-G-A

7856638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101640-G-C

7857167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36101201-G-A

7857186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36101182-C-T

7857267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36101119-G-T

7857271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36101117-G-A

7857337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36101059-C-T

http://identifiers.org/hco/4/GRCh38#7857391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36101006-C-A

7857550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36100878-C-T

7857555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36100863-C-T

7857563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36100838-T-C

7857571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36100830-T-C

7857757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36100627-T-C

7857766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36100618-T-C

7857807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36100598-G-A

7857866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36100526-A-G

7860871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36099192-C-T

7861189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36098931-A-G

7861241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36098881-G-A

7861384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36098755-T-C

7861426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36098667-T-C

http://identifiers.org/hco/4/GRCh38#7861757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36098405-C-A

7861757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36098405-C-T

7861974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36098226-T-C

7867962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36094024-G-A

7868120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093860-T-A

7868120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093860-T-G

http://identifiers.org/hco/4/GRCh38#7868127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36093849-A-C

7868152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093824-T-C

7868397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093660-G-A

7868412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093645-T-C

7868460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093630-T-C

7868460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093630-T-G

7868501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093589-T-A

7868501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093589-T-C

7868501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093589-T-G

7868502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093588-G-A

7868502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093588-G-C

7868502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093588-G-T

7868551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093546-A-G

7868605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093491-G-A

7868605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093491-G-T

http://identifiers.org/hco/4/GRCh38#7868611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36093485-C-A

7868611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093485-C-T

7868644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36093452-G-A

7868689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36093410-T-C

7868689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36093410-T-G

7868762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093337-G-A

7868762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093337-G-T

7868778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093329-C-G

7868778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093329-C-T

7868839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093277-T-A

7868911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093171-T-A

7868911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093171-T-C

7868923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093158-A-T

7871872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36093089-T-C

7871982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36092992-T-C

7872026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: missense variant
orthologous variants: 36092948-T-G

http://identifiers.org/hco/4/GRCh38#7872166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36092796-C-A

7872166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36092796-C-G

7872166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36092796-C-T

7872222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36092734-A-G

http://identifiers.org/hco/4/GRCh38#7872233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36092723-C-A

7872233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36092723-C-G

7872233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36092723-C-T

7872236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36092720-A-G

http://identifiers.org/hco/4/GRCh38#7872306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36092655-A-C

7872306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36092655-A-G

7872306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36092655-A-T

7872391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, undefined
orthologous variants: 36092581-A-G

7872391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, undefined
orthologous variants: 36092581-A-T

7879239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089557-A-T

7879319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089476-C-T

7879435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089377-G-A

7879476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089338-T-C

7879496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089318-T-A

7885596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089166-G-A

7885610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089161-A-T

7885660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089114-T-C

7885700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089077-G-C

7885772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36089007-A-G

7885894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088897-G-C

7886154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088631-T-C

7886275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088552-A-G

7886275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088552-A-T

7886319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088520-T-G

http://identifiers.org/hco/4/GRCh38#7886360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36088503-A-C

7886510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088306-T-G

http://identifiers.org/hco/4/GRCh38#7886568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36088110-A-C

7886573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088105-G-T

7886575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36088103-G-A

7886741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36087945-T-C

7886802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36087902-G-C

7886850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36087851-T-C

7886996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36087692-A-G

7890555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36085634-C-G

7890555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36085634-C-T

7890732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, undefined
orthologous variants: 36085451-C-G

7890990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, undefined
orthologous variants: 36085236-C-T

7891167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36085085-A-G

7891251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36085024-C-T

7891290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36084997-A-T

http://identifiers.org/hco/4/GRCh38#7891403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36084908-A-C

7894799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36082827-C-T

7895441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36082265-C-T

7895535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36082174-C-T

7899214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080663-G-A

7899214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080663-G-C

7899280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080600-C-T

7899326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080562-T-G

7899379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080508-T-A

7899379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080508-T-C

http://identifiers.org/hco/4/GRCh38#7899382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36080505-C-A

7899382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080505-C-G

7899382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080505-C-T

7899802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36080144-A-G

7899997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079953-T-C

7900093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079881-T-C

http://identifiers.org/hco/4/GRCh38#7900417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36079666-A-C

7900417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079666-A-G

7900550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079552-T-C

7900836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079281-C-G

7900842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079275-A-T

7900922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36079198-G-A

7901165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078982-A-T

7901260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078907-G-A

7901260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078907-G-C

7901477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078769-C-G

7901557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078727-C-G

7901571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078713-A-G

7901749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078546-C-T

7901778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36078520-A-G

7901963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077985-C-T

7901994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077934-T-G

7902000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077928-T-C

7902011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077917-A-T

7902041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077873-G-A

http://identifiers.org/hco/4/GRCh38#7902476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36077444-A-C

7902476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077444-A-G

7902492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077429-T-C

7902593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36077342-A-G

7903074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36076892-G-C

7903765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36076338-T-C

7903795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36076309-T-C

7903980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36076141-T-G

7904063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36076058-G-C

7905242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36073425-T-C

http://identifiers.org/hco/4/GRCh38#7907091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36071362-C-A

http://identifiers.org/hco/4/GRCh38#7907154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36071301-A-C

7909216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36067299-C-T

7909582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36066957-G-T

7909801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36066771-C-G

7909843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36066744-A-G

7910199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36066354-A-T

7910353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36066254-G-A

http://identifiers.org/hco/4/GRCh38#7910405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36066224-C-A

7910664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36066056-C-T

7910802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36065890-G-A

7910804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36065888-T-C

7911387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36065297-G-T

7911393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36065291-A-G

7932392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36057712-T-C

7934286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36055909-G-T

7934303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36055908-C-G

7934566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36055752-T-C

7934828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36055492-C-T

7935171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36055173-C-T

7935363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36055006-C-T

7935379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054988-T-A

7935388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054979-C-G

7935455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054914-T-C

7935545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054849-C-T

7935648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054761-G-A

http://identifiers.org/hco/4/GRCh38#7935655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36054754-C-A

7935655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054754-C-T

7935718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054689-A-G

7935786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054646-G-A

7935839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054619-T-C

7936172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054430-C-T

7936173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054429-T-C

7936285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36054326-A-G

7937843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36053121-T-C

7937913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36053071-G-C

7938891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36052030-G-A

7938891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36052030-G-T

7938899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36052015-G-T

7938991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36051922-G-A

7938991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36051922-G-C

7938991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron variant
orthologous variants: 36051922-G-T

http://identifiers.org/hco/4/GRCh38#7939114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051772-C-A

7939114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051772-C-G

7939114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051772-C-T

7939260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051643-G-A

7939260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051643-G-C

7939260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051643-G-T

http://identifiers.org/hco/4/GRCh38#7939287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051600-C-A

7939287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051600-C-T

http://identifiers.org/hco/4/GRCh38#7939299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051548-C-A

7939299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051548-C-T

http://identifiers.org/hco/4/GRCh38#7939313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051534-C-A

http://identifiers.org/hco/4/GRCh38#7939395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051443-C-A

7939395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051443-C-G

7939395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051443-C-T

http://identifiers.org/hco/4/GRCh38#7939412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051423-C-A

7939420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051389-A-G

http://identifiers.org/hco/4/GRCh38#7939536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051223-C-A

7939536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051223-C-T

7939544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051214-A-G

http://identifiers.org/hco/4/GRCh38#7939570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36051191-C-A

7939570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36051191-C-T

7939661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36050980-G-A

http://identifiers.org/hco/4/GRCh38#7939799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36050768-C-A

7939799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36050768-C-T

7939809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36050758-T-C

http://identifiers.org/hco/4/GRCh38#7939857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36050720-C-A

7939857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36050720-C-T

7939859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36050718-G-A

7939859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36050718-G-C

7939859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24017
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36050718-G-T