78759215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 3 prime UTR variant
orthologous variants: 90082144-G-A

78759215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 3 prime UTR variant
orthologous variants: 90082144-G-T

78759342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 3 prime UTR variant
orthologous variants: 90082021-G-C

78759342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 3 prime UTR variant
orthologous variants: 90082021-G-T

http://identifiers.org/hco/15/GRCh38#78759412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90081942-C-A

78759412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 3 prime UTR variant
orthologous variants: 90081942-C-T

78759443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90081900-T-C

78759448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90081895-T-A

78759451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90081892-G-A

78759451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90081892-G-C

78759451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90081892-G-T

78759499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90081844-G-A

78759499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90081844-G-T

http://identifiers.org/hco/15/GRCh38#78759625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90081704-C-A

78759625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081704-C-T

78759656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081645-T-C

78759826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081502-C-T

78759899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081425-C-G

78759912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081412-T-C

78759998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081335-C-G

78759998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081335-C-T

78760023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081309-T-C

78760063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081252-G-A

78760122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081210-C-T

78760169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081157-G-A

78760184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90081142-A-G

http://identifiers.org/hco/15/GRCh38#78760218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90081098-C-A

78760338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080978-A-G

78760548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080788-G-A

78760548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080788-G-T

78760735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080591-C-T

78760766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080557-C-T

78760958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080379-T-C

78760959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080378-C-T

78760974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080368-T-C

78760988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080354-C-G

78760988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080354-C-T

78761032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080303-G-T

78761161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080179-C-G

78761194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080136-G-A

78761219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90080111-T-G

http://identifiers.org/hco/15/GRCh38#78761618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079764-A-C

78762261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079334-T-C

78762297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079302-T-C

78762316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079286-G-T

http://identifiers.org/hco/15/GRCh38#78762358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079248-C-A

78762358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079248-C-T

http://identifiers.org/hco/15/GRCh38#78762365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079241-C-A

78762365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079241-C-T

78762396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90079222-G-A

78762396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90079222-G-T

78762408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90079208-G-A

78762408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90079208-G-T

78762411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90079205-T-A

78762411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90079205-T-C

http://identifiers.org/hco/15/GRCh38#78762412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079204-C-A

78762412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90079204-C-T

http://identifiers.org/hco/15/GRCh38#78762501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079115-C-A

78762501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90079115-C-T

http://identifiers.org/hco/15/GRCh38#78762519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079097-C-A

http://identifiers.org/hco/15/GRCh38#78762569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079047-A-C

78762569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90079047-A-G

78762569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90079047-A-T

http://identifiers.org/hco/15/GRCh38#78762589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079030-A-C

78762589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079030-A-G

78762589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079030-A-T

78762615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079004-T-A

78762615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90079004-T-C

http://identifiers.org/hco/15/GRCh38#78762627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078976-C-A

78762627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078976-C-G

78762627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078976-C-T

78762826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078865-G-A

78762827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078864-G-A

78762918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078822-G-A

78762962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078783-G-A

78762976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078776-G-A

http://identifiers.org/hco/15/GRCh38#78763450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078367-A-C

78763450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078367-A-T

78763492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078327-C-T

http://identifiers.org/hco/15/GRCh38#78763607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078223-C-A

78763607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078223-C-G

78763607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078223-C-T

78763652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078182-G-A

78763652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078182-G-T

http://identifiers.org/hco/15/GRCh38#78763664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078170-A-C

http://identifiers.org/hco/15/GRCh38#78763669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078162-C-A

78763669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90078162-C-T

78763784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90078043-A-T

78763852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90077975-G-A

78763852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90077975-G-T

http://identifiers.org/hco/15/GRCh38#78763907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077920-C-A

78763907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90077920-C-T

78763942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90077885-G-A

78763942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90077885-G-T

http://identifiers.org/hco/15/GRCh38#78763978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077849-C-A

78763978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077849-C-T

78763984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077843-G-A

78763984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077843-G-C

78763984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077843-G-T

78763994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90077833-T-A

78763994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077833-T-C

78763999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077828-G-A

78763999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077828-G-T

http://identifiers.org/hco/15/GRCh38#78764223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077625-C-A

78764223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077625-C-T

78764372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077506-G-C

78764403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077473-T-A

78764403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077473-T-C

78764403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077473-T-G

http://identifiers.org/hco/15/GRCh38#78764436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077450-A-C

78764436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077450-A-G

78764455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077429-G-A

78764455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077429-G-T

78764478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077399-T-A

78764478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077399-T-C

78764481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077396-G-C

78764481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077396-G-T

78764570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90077346-T-C

78764619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077297-G-A

78764619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077297-G-T

78764631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077285-G-T

http://identifiers.org/hco/15/GRCh38#78764669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077247-C-A

78764669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90077247-C-G

78764669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90077247-C-T

78764682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077234-G-A

78764682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90077234-G-T

http://identifiers.org/hco/15/GRCh38#78764716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077200-C-A

78764716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077200-C-T

http://identifiers.org/hco/15/GRCh38#78764723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077193-C-A

http://identifiers.org/hco/15/GRCh38#78764814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077151-C-A

78764814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077151-C-T

http://identifiers.org/hco/15/GRCh38#78764867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077108-C-A

78764867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077108-C-G

78765040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076996-A-G

78765051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076989-G-A

78765051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076989-G-C

78765051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076989-G-T

http://identifiers.org/hco/15/GRCh38#78765066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076974-C-A

78765066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076974-C-T

78765116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076946-C-T

http://identifiers.org/hco/15/GRCh38#78765135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076929-C-A

78765135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076929-C-T

78765145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076919-G-C

78765178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076904-A-G

78765188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076894-G-A

78765188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076894-G-C

78765188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076894-G-T

78765225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076863-G-A

78765225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076863-G-T

78765253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076834-G-T

78765470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076605-C-T

http://identifiers.org/hco/15/GRCh38#78765492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076547-C-A

78765522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076432-A-T

78765528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076426-T-C

78765545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076406-G-C

78765545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076406-G-T

http://identifiers.org/hco/15/GRCh38#78765557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076399-C-A

78765557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076399-C-T

78765595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076373-T-A

http://identifiers.org/hco/15/GRCh38#78765596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076372-C-A

78765596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron variant
orthologous variants: 90076372-C-T

78765701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90076264-G-A

http://identifiers.org/hco/15/GRCh38#78766048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075938-C-A

78766048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075938-C-G

78766048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075938-C-T

78766069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075917-C-G

http://identifiers.org/hco/15/GRCh38#78766112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075874-C-A

78766112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075874-C-T

78766151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075835-T-C

78766162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075824-T-C

http://identifiers.org/hco/15/GRCh38#78766175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075811-C-A

78766175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075811-C-G

78766175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075811-C-T

78766182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075804-C-G

78766182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90075804-C-T

78766200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90075786-G-A

78766200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075786-G-T

78766343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075649-G-A

78766343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075649-G-C

http://identifiers.org/hco/15/GRCh38#78766452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075540-C-A

http://identifiers.org/hco/15/GRCh38#78766478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075514-A-C

78766478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075514-A-G

78766478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075514-A-T

78766500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90075495-G-A

78766681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075314-G-C

78766681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075314-G-T

78766747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075248-G-A

78766747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense variant
orthologous variants: 90075248-G-T

78766794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: synonymous variant
orthologous variants: 90075207-G-T

78766840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90075161-T-C

78767110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074900-G-A

78767110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074900-G-T

78767111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074899-G-T

http://identifiers.org/hco/15/GRCh38#78767126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074884-A-C

78767126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074884-A-G

78767131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074879-T-C

78767131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074879-T-G

http://identifiers.org/hco/15/GRCh38#78767193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074818-A-C

78767193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074818-A-G

78767193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074818-A-T

78767340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074685-G-A

78767613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074421-G-A

78767632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074403-C-G

78767632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074403-C-T

78767641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074394-T-C

http://identifiers.org/hco/15/GRCh38#78767650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074382-A-C

78767667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074365-G-C

78767667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074365-G-T

http://identifiers.org/hco/15/GRCh38#78767683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074345-C-A

78767687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074341-G-A

78767699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074329-G-C

78767745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074291-A-G

http://identifiers.org/hco/15/GRCh38#78768014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074060-C-A

78768148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90073998-T-C

78768268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073878-C-G

78768268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073878-C-T

78768377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073794-G-T

78768394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073777-A-G

78768403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073768-G-A

78768403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073768-G-T

78768416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073758-G-A

78768416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90073758-G-T

78768921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90075207-G-A

78768967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90075161-C-T

78771221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073492-G-A

78771221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073492-G-T

78771233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073480-T-C

78771248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073471-T-A

78771333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073385-C-T

78771456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073251-G-A

78771456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073251-G-T

78771566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073162-G-C

78771566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073162-G-T

http://identifiers.org/hco/15/GRCh38#78771568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90073160-C-A

78771568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073160-C-T

78771576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073152-G-A

78771576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073152-G-T

78771601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90073127-T-A

78771841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072889-G-C

78771841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072889-G-T

http://identifiers.org/hco/15/GRCh38#78771861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90072871-C-A

78771861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072871-C-T

78771895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072846-C-G

78771895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072846-C-T

http://identifiers.org/hco/15/GRCh38#78771955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90072776-C-A

78772138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072596-C-T

http://identifiers.org/hco/15/GRCh38#78772223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90072523-C-A

78772309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072474-G-A

78772336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072444-C-T

78772350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072430-C-T

78772490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072337-T-C

78772589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072240-G-C

78772704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90072115-T-G

http://identifiers.org/hco/15/GRCh38#78772726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90072090-C-A

78772935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071922-G-A

78772935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071922-G-T

http://identifiers.org/hco/15/GRCh38#78772965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90071884-C-A

78772965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071884-C-T

78772985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071866-G-A

78772985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071866-G-T

78772996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071855-G-A

78772996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071855-G-C

78772996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071855-G-T

78773031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071842-G-A

78773031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071842-G-T

http://identifiers.org/hco/15/GRCh38#78773257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90071622-C-A

78773257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071622-C-T

http://identifiers.org/hco/15/GRCh38#78773338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90071555-C-A

78773380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071516-A-G

78773380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071516-A-T

78773403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071487-A-G

78773422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071468-T-C

78773509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071380-G-A

78773509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071380-G-T

78773644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071271-T-G

78773776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071153-T-C

78773860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90071100-T-C

http://identifiers.org/hco/15/GRCh38#78774039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90070935-C-A

78774039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070935-C-T

78774040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070934-C-T

78774044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070930-G-A

78774044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070930-G-C

78774070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070922-C-T

78774097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070896-A-G

78774097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070896-A-T

78774139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070870-G-T

78774145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070864-G-T

78774225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90070785-C-T

78774241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90070769-C-T

http://identifiers.org/hco/15/GRCh38#78774324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90070686-A-C

78774324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070686-A-G

78774327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070682-A-G

78774353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070655-G-A

78774353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070655-G-T

http://identifiers.org/hco/15/GRCh38#78774367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90070641-C-A

78774371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070637-T-C

http://identifiers.org/hco/15/GRCh38#78774475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90070603-C-A

78774475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070603-C-G

78774475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070603-C-T

http://identifiers.org/hco/15/GRCh38#78774489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90070589-C-A

78774489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070589-C-G

78774489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070589-C-T

78774500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070576-G-T

78774563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070547-C-G

78774563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070547-C-T

78774587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070526-T-C

78774716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90070397-C-T

78774757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90070356-G-C

http://identifiers.org/hco/15/GRCh38#78774825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90070302-C-A

78774825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070302-C-G

78774825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90070302-C-T

78775382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069831-G-A

78775487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069735-G-A

78775774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069519-C-T

78775897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069387-C-G

78775897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069387-C-T

78775956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069329-T-C

78776008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069279-C-T

78776044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069249-T-C

78776111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90069182-G-A

78776194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90069112-T-C

http://identifiers.org/hco/15/GRCh38#78776368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90068945-C-A

78776368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068945-C-G

http://identifiers.org/hco/15/GRCh38#78776485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90068843-C-A

78776485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068843-C-T

78776516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068806-G-A

78776516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068806-G-C

78776516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068806-G-T

78776621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068744-T-C

78776653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068714-A-G

78776658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068709-G-A

78776658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068709-G-T

78776706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068650-G-A

78776706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068650-G-T

78776722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068631-A-G

78776722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068631-A-T

78776724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068629-T-C

78776860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068496-G-A

78776860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068496-G-T

78776887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068467-G-A

78776887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068467-G-T

78776894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068460-C-G

http://identifiers.org/hco/15/GRCh38#78776895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90068459-C-A

78776895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068459-C-T

http://identifiers.org/hco/15/GRCh38#78776928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90068428-C-A

78776928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068428-C-T

78776930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068426-T-A

78776930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068426-T-C

78776989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068374-T-G

78776995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068368-C-T

78777170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068172-T-A

78777170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068172-T-C

http://identifiers.org/hco/15/GRCh38#78777284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90068066-C-A

78777284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068066-C-G

http://identifiers.org/hco/15/GRCh38#78777322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90068028-A-C

78777322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068028-A-G

78777322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90068028-A-T

78777371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90067976-G-A

78777371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90067976-G-T

http://identifiers.org/hco/15/GRCh38#78777379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90067968-A-C

78777472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90067903-G-A

78777472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90067903-G-C

78777522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90067853-T-A

78777522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90067853-T-C

78777596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90067774-T-A

http://identifiers.org/hco/15/GRCh38#78777624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90067731-C-A

78777624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067731-C-G

78777624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067731-C-T

78777627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067730-G-A

78777627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067730-G-T

78777629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067728-G-A

78777629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067728-G-T

78777688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067683-A-G

http://identifiers.org/hco/15/GRCh38#78777777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90067601-C-A

78777901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067471-C-T

78778048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067375-A-G

http://identifiers.org/hco/15/GRCh38#78778360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90067144-C-A

78778360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067144-C-T

78778362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067142-C-T

78778598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90067000-T-A

78778740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90066896-C-T

http://identifiers.org/hco/15/GRCh38#78778745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90066891-C-A

78780098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90066467-T-C

78780818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90066051-C-T

78781237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90065678-T-C

78781300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90065631-G-A

78781311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90065622-G-T

78781429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90065507-G-A

78782473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064780-C-G

78782473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064780-C-T

78782525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064735-C-T

78782575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064687-G-T

78782765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064489-C-T

78782940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064417-T-C

78782961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90064397-C-T

78788411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062640-G-A

78788411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062640-G-T

78788527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062533-C-T

78788553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062507-T-C

78788557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062503-A-G

78788877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062195-A-G

78788885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90062187-T-C

78789179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061988-C-T

78789181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061986-G-T

78789280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061917-T-C

78789569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061641-C-T

78789595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061615-T-C

78789674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061538-G-A

78789674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90061538-G-C

78789821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90061391-G-T

http://identifiers.org/hco/15/GRCh38#78789842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90061370-C-A

78789842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90061370-C-T

http://identifiers.org/hco/15/GRCh38#78789876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90061339-C-A

78790694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90060304-T-C

78790796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 90060202-T-C

78790866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90060133-A-G

78790890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90060109-G-A

78790890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90060109-G-T

http://identifiers.org/hco/15/GRCh38#78790946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90060072-C-A

78790946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90060072-C-T

78791026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90060014-G-A

78791026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90060014-G-T

78791060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059984-G-A

78791060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059984-G-C

78791061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059983-A-G

http://identifiers.org/hco/15/GRCh38#78791068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90059977-C-A

78791068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059977-C-T

78791263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059788-A-T

http://identifiers.org/hco/15/GRCh38#78791303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90059758-C-A

78791329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059734-C-G

78791329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059734-C-T

http://identifiers.org/hco/15/GRCh38#78791333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90059730-C-A

http://identifiers.org/hco/15/GRCh38#78791347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90059716-C-A

78791347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059716-C-T

http://identifiers.org/hco/15/GRCh38#78791368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90059693-C-A

78791374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059687-A-G

78791434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90059626-T-C

78795365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90058284-G-A

78795548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90058127-C-T

http://identifiers.org/hco/15/GRCh38#78796022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90057273-C-A

78796147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90057177-T-C

78796227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90057114-G-A

78796344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90057004-C-G

78796367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056974-T-C

78796419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056878-C-G

78796482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056818-A-T

78796499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056801-A-G

http://identifiers.org/hco/15/GRCh38#78796519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90056780-C-A

78796540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056762-C-G

78796732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90056577-C-T

78797515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056464-T-A

78797562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056420-G-T

78797608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056374-C-T

78797801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056210-A-G

78797833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90056178-T-C

78797857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055923-G-T

http://identifiers.org/hco/15/GRCh38#78797916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90055856-C-A

78797916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055856-C-T

78797938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055850-A-G

http://identifiers.org/hco/15/GRCh38#78797982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90055804-A-C

78797982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90055804-A-G

http://identifiers.org/hco/15/GRCh38#78798153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90055633-C-A

http://identifiers.org/hco/15/GRCh38#78798156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90055630-C-A

78798156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055630-C-T

78798251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055536-T-G

http://identifiers.org/hco/15/GRCh38#78798259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90055528-C-A

78798260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055527-T-A

78798260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055527-T-C

78798260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055527-T-G

78798261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055526-G-A

78798261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055526-G-T

78798428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90055369-C-G

78798428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90055369-C-T

78798562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90055230-T-G

78798713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055079-C-T

78798755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90055046-C-G

http://identifiers.org/hco/15/GRCh38#78798807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90054994-A-C

78798816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054985-T-C

78798842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054962-A-G

78798907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054901-G-A

78798913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054895-G-C

78798915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054893-G-A

78799461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054427-G-A

78799981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054044-C-G

78800026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90054020-A-G

78800177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053895-T-A

78800217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053855-G-A

78800217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053855-G-C

78800217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053855-G-T

78800272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053800-G-C

78800272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053800-G-T

78800290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053782-G-T

http://identifiers.org/hco/15/GRCh38#78800293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90053779-C-A

78800293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053779-C-G

78800293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053779-C-T

78800302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90053770-G-A

78800302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053770-G-T

78800403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053669-T-C

78800523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053549-G-A

http://identifiers.org/hco/15/GRCh38#78800527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90053545-C-A

78800527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053545-C-T

78800538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053534-G-A

78800538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90053534-G-T

78800553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90053519-G-A

78800553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90053519-G-T

78800592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053483-G-A

78800592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053483-G-C

78800592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053483-G-T

78800593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053482-G-A

78800593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053482-G-T

78800600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053475-C-G

78800600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053475-C-T

78800797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053193-A-G

78800955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053137-G-A

http://identifiers.org/hco/15/GRCh38#78800982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90053119-A-C

78800990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053111-C-G

78801007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053095-C-G

78801019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90053083-G-A

78801112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90052975-C-T

78801117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90052970-T-A

78801117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90052970-T-C

78801145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90052942-T-G

78802237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90051178-C-T

78802490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90050946-G-C

78802519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90050922-A-G

78802595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90050845-T-G

78803944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90049698-G-A

78804229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90049443-T-C

78804443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90049028-A-G

78804531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90048935-T-C

78804860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90048629-G-A

78808660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90047470-T-C

78808756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90047374-C-T

78808846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90047290-G-T

78808878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90047258-T-C

78809137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90047082-C-T

78809164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90047059-T-C

78809416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046825-G-A

78809441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046797-G-A

78809441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046797-G-C

78809521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046698-G-A

78809588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046629-T-C

78809670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046554-G-A

78810140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90046232-T-G

78810403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90045995-C-T

78810417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90045981-G-A

http://identifiers.org/hco/15/GRCh38#78810463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045931-C-A

78810463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90045931-C-T

78810466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90045928-C-T

78810558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045841-A-G

78810558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045841-A-T

78810585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045815-A-G

http://identifiers.org/hco/15/GRCh38#78810615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045796-C-A

78810615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045796-C-G

78810615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045796-C-T

http://identifiers.org/hco/15/GRCh38#78810663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045769-C-A

78810669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045763-G-A

78810669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045763-G-T

78810726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045706-G-A

78810726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045706-G-T

78810738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045693-A-G

78810856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045584-G-T

http://identifiers.org/hco/15/GRCh38#78810923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045517-C-A

78810923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045517-C-T

http://identifiers.org/hco/15/GRCh38#78810957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045483-A-C

78810957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045483-A-G

78810986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045458-G-A

78810986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045458-G-C

78810986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90045458-G-T

78811104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90045382-G-A

78811104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90045382-G-T

78811131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90045355-T-C

78811143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90045343-G-A

78811143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90045343-G-C

78811143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90045343-G-T

78811208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90045308-G-A

78811208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90045308-G-T

http://identifiers.org/hco/15/GRCh38#78811237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045279-C-A

78811237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90045279-C-T

http://identifiers.org/hco/15/GRCh38#78811352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90045167-C-A

78811363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 223
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90045149-T-C