117455535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52095760-G-A

117455564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52095789-T-G

117455863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096066-C-T

117455879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096082-A-T

117455921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52096124-A-G

117456368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52097326-A-G

117456949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100012-A-G

117457007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100081-T-A

117457044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52100115-C-G

http://identifiers.org/hco/6/GRCh38#117457148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52100224-A-C

117479903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52104000-T-C

117480210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52104294-A-G

117480558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52105842-T-G

117480587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52105871-C-T

117480749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52106017-G-A

117480749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52106017-G-C

117480787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52106043-G-A

117480811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52106063-G-T

117480879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non coding transcript exon variant
orthologous variants: 52106136-G-C

117480971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non coding transcript exon variant
orthologous variants: 52107679-T-G

117481488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52108705-G-A

117481488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52108705-G-C

http://identifiers.org/hco/6/GRCh38#117481560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#52108789-A-C

117481560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52108789-A-T

117481881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109071-T-C

117481881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109071-T-G

117481921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109114-T-C

117482019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109184-G-A

117482123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109283-A-G

117482494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109602-G-A

117482494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109602-G-C

117482494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109602-G-T

117482512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109619-T-A

117482512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109619-T-G

http://identifiers.org/hco/6/GRCh38#117482532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52109639-C-A

117482532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109639-C-G

117482532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109639-C-T

117482533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109640-G-A

117482533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109640-G-C

117482533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109640-G-T

117482548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109653-G-A

117482548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109653-G-T

http://identifiers.org/hco/6/GRCh38#117482586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52109667-C-A

117482586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109667-C-T

117482623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109710-G-T

http://identifiers.org/hco/6/GRCh38#117482673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#52109735-C-A

117482673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52109735-C-G

117482673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52109735-C-T

117482680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52109742-G-A

117482689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109751-T-A

http://identifiers.org/hco/6/GRCh38#117482725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52109792-C-A

117482725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109792-C-T

http://identifiers.org/hco/6/GRCh38#117482750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52109815-C-A

117482750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109815-C-G

117482750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109815-C-T

117482779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109844-G-A

117482779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109844-G-C

117482779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52109844-G-T

117482841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52109879-G-A

117482841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52109879-G-T

117482923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109942-G-A

117482923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109942-G-C

117482923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109942-G-T

117482930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109949-G-A

117482930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109949-G-T

http://identifiers.org/hco/6/GRCh38#117482936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52109955-A-C

117482936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109955-A-G

117482936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52109955-A-T

117483031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110004-T-C

117483134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110082-A-G

117483717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110533-A-T

117483723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110539-G-A

117483870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52110708-A-G

117484640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111816-C-T

117484648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52111824-C-G

http://identifiers.org/hco/6/GRCh38#117484876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52113275-C-A

http://identifiers.org/hco/6/GRCh38#117484932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52113307-C-A

117484932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113307-C-G

117485120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113456-A-G

117485133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113469-C-T

117485134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113470-G-A

117485134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113470-G-T

117485160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52113496-T-C

117485246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114032-C-T

117485254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114041-G-C

117485612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114391-G-C

117485619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114398-A-T

117485718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114498-A-G

117485758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114538-G-A

http://identifiers.org/hco/6/GRCh38#117485992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52114767-A-C

117486116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52114884-G-A

117486308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115373-T-C

117486474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115956-G-C

117486491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52115970-G-A

117486607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116070-A-G

117486665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116131-T-C

117486696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116154-G-T

117487247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116707-A-G

117487265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116724-G-T

117487283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116742-G-A

117487363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116835-C-T

117487410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116868-G-C

117487489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52116935-T-G

117487695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117041-G-A

117487801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117138-T-A

117487846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117173-A-G

117487877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117204-G-T

117487900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117229-G-T

117488230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117574-G-A

117488284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117645-T-C

117488300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52117663-T-A

117488669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52118200-T-C

117488674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52118205-A-G

117488682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52118211-G-A

117488697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52118225-C-T

117488847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52118343-T-C

117492272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52118737-G-C

117492541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119003-G-C

117492804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119241-C-T

117492838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119273-T-C

117493059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119462-A-G

117493172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119725-G-A

117493263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52119817-T-A

117493460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120150-C-T

117493625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120537-C-T

117493640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120552-C-T

117493717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120626-G-A

117493805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52120697-C-G

117494460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124005-G-A

117494507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124050-C-T

117494550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124091-T-C

117494680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124471-G-T

117494724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52124933-G-A

117494859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52125067-A-T

http://identifiers.org/hco/6/GRCh38#117494866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52125074-C-A

117494879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52125087-A-T

117494894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52125101-G-A

117494916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52125123-G-T

http://identifiers.org/hco/6/GRCh38#117494931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52125138-C-A

117494931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52125138-C-T

117496088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128755-G-C

117496108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52128784-A-G

117496510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129618-A-T

117496584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52129692-A-G

117496929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130009-G-A

117496929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52130009-G-C

http://identifiers.org/hco/6/GRCh38#117497329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52132033-C-A

117497329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132033-C-T

117497343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52132047-T-C

117498243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52134385-G-T

117498315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52134460-G-A

117498321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52134466-T-G

117498768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52134970-C-G

117498785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135008-C-T

117501091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135355-G-C

117501091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135355-G-T

117501141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135403-G-A

117501196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135450-G-C

117501722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135643-C-T

117501986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135857-C-G

117501986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135857-C-T

117502029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135881-G-A

117502113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135922-C-G

117502113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135922-C-T

117502135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135943-G-A

117502149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135957-C-G

117502149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52135957-C-T

117503614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52137655-T-C

117503632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52137672-T-C

117503657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52137697-T-C

http://identifiers.org/hco/6/GRCh38#117503858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#52137914-C-A

117503858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52137914-C-G

117503858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52137914-C-T

117503945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52138001-C-G

117503945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52138001-C-T

117504064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138109-T-C

117504064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138109-T-G

http://identifiers.org/hco/6/GRCh38#117504102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52138147-A-C

117504191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138239-C-G

117504314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138350-A-G

117504381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138419-G-C

117504381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138419-G-T

117504416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138437-A-G

117504465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138476-C-T

117504490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138497-G-A

117504548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52138545-T-G

117505914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139302-T-A

http://identifiers.org/hco/6/GRCh38#117505921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52139312-C-A

117505921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139312-C-T

117506184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52139532-A-G

117506392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139853-G-A

117506400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139861-C-G

117506400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139861-C-T

117506416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139877-C-G

117506495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139929-T-C

117506527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52139960-T-G

117506939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52140276-C-T

117506968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52140305-G-A

117506973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52140310-T-A

117507022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52140359-A-T

http://identifiers.org/hco/6/GRCh38#117510275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52148177-C-A

117510275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148177-C-T

117510289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148211-C-T

http://identifiers.org/hco/6/GRCh38#117510306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52148228-C-A

117510342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148267-G-C

117510342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148267-G-T

117510823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148760-C-T

117510831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148768-G-T

117510840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52148777-A-T

117510920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149026-A-T

117510955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149069-A-G

117511029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52149139-C-G

117511987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150061-A-G

117512071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150143-C-T

117512359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150388-G-A

117512495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150522-C-T

117512865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150911-A-G

117512981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52150989-A-T

117513247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151181-G-A

117513459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151333-C-T

117513511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151380-C-T

117513563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151431-T-C

117513566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151434-T-C

117513654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151729-C-T

117513856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52151960-T-G

117514155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156012-G-T

117514177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156043-A-G

117514215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52156083-G-T

117516401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52158117-C-T

117516402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52158118-G-A

117519109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159124-G-A

117519152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52159168-A-T

117519669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160069-G-A

117519708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160108-A-G

117519709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160109-T-C

117519731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160131-G-T

http://identifiers.org/hco/6/GRCh38#117519763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52160147-C-A

117519763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160147-C-T

117519796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160179-C-T

117519800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160183-T-C

117519801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160184-G-A

117519916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52160299-T-A

117519940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52160323-C-T

117519985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160357-T-C

117520011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160373-A-G

117520068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160439-G-A

117520452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160721-G-C

117520531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160801-C-T

117520555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160825-G-A

117520765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52160982-G-C

117520805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52161022-G-A

117520812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52161029-A-G

117521319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52162245-T-A

117521377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52162299-A-G

117521416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52162339-G-T

http://identifiers.org/hco/6/GRCh38#117521493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52162412-C-A

117522231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163470-G-A

117522774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163713-G-A

117522946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52163866-A-G

117523519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164388-A-G

117523521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164390-A-G

http://identifiers.org/hco/6/GRCh38#117523522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52164391-C-A

117523803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164662-A-G

117523803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52164662-A-T

117523963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52165157-T-A

http://identifiers.org/hco/6/GRCh38#117523968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52165162-A-C

117523968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52165162-A-G

117524712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166036-G-C

117524809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166131-T-C

117524912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166229-C-T

117525175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166457-T-C

117525300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166890-A-G

117525318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166913-G-A

117525318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166913-G-T

117525348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166933-T-C

117525425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52167010-A-G

http://identifiers.org/hco/6/GRCh38#117525483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52167056-C-A

117525483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167056-C-T

117525515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167088-G-A

117525515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167088-G-T

117525544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167117-T-C

117525647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167229-G-C

117525647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52167229-G-T

117525751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168274-A-G

117525751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52168274-A-T

http://identifiers.org/hco/6/GRCh38#117525952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52168472-C-A

117526319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169257-A-G

117526670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169462-A-G

117526760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169517-G-A

117526795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52169535-T-C

117528011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52171737-A-G

http://identifiers.org/hco/6/GRCh38#117529161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52166417-C-A

117529161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166417-C-T

117529250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166509-A-G

117529313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52166890-A-G

117529535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176238-G-C

117529572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176266-G-A

117529588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176294-A-G

117529909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176553-G-A

117529966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176589-C-T

http://identifiers.org/hco/6/GRCh38#117530059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52176684-A-C

117530164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52176776-C-G

117530954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179058-C-T

117531019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179107-A-G

117531511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179808-G-C

117531635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52179930-G-C

117531978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180230-T-C

117532010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180236-G-A

http://identifiers.org/hco/6/GRCh38#117532123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52180455-C-A

117532123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180455-C-T

117532146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180496-G-A

117532146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180496-G-T

117532168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180551-C-T

117532217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180645-T-C

117532457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180876-A-G

117532504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52180923-T-C

http://identifiers.org/hco/6/GRCh38#117532532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52181055-A-C

117532573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52181219-A-G

http://identifiers.org/hco/6/GRCh38#117532997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52181835-A-C

117533068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52181903-C-T

117533245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52182134-T-C

117534751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185060-T-C

117534864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185138-C-G

117535289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185577-C-T

117535364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185675-G-A

117535417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52185727-C-G

117537197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52187508-A-G

117537234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52187545-C-T

117542452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

117542453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

117542525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

117542690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

117543095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52188887-G-A

117543167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52188953-T-A

http://identifiers.org/hco/6/GRCh38#117543778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52189618-C-A

117543813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52189660-C-T

117543859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52189700-G-C

117543994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52189836-T-G

117544222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52190127-G-A

117544222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52190127-G-C

117544449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52190371-A-G

117544465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52190387-A-G

http://identifiers.org/hco/6/GRCh38#117544524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52190447-A-C

117544524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 52190447-A-G

117544640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52191791-T-C

http://identifiers.org/hco/6/GRCh38#117544717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52191858-C-A

117544749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52191901-T-C

http://identifiers.org/hco/6/GRCh38#117544960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52192085-C-A

http://identifiers.org/hco/6/GRCh38#117545334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#52192990-C-A

117545334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52192990-C-T

117545357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52193009-A-G

117545363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52193015-A-G

117545430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52193085-C-T

117545599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 52193249-T-G

117545607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52193257-A-G

http://identifiers.org/hco/6/GRCh38#117545626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52193279-A-C

117545626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193279-A-G

117545634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193283-G-T

117545654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193303-A-G

117545656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193311-G-A

117545656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193311-G-T

117545657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193312-G-A

117545657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193312-G-T

117545659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193314-G-A

117545659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193314-G-C

117545664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193319-G-A

117545730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193375-T-A

117545730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52193375-T-G

117547838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52195509-C-T

117547841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52195512-C-T

117547854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52195525-C-G

117547854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52195525-C-T

117547868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52195539-T-G

117547874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52195545-G-A

117548148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52195813-C-T

117548187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52195852-C-T

117548236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52195898-G-A

http://identifiers.org/hco/6/GRCh38#117548286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#52195948-C-A

117548286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52195948-C-T

117548393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196046-A-G

117548402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196055-C-T

117548449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196102-G-A

117548449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196102-G-C

117548643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196250-G-A

117548643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196250-G-T

http://identifiers.org/hco/6/GRCh38#117548647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52196255-C-A

117548647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196255-C-T

117548656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196264-G-T

117548793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196382-C-G

117548793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196382-C-T

117548818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196402-G-T

117548924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196496-G-A

117548986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196552-T-C

http://identifiers.org/hco/6/GRCh38#117548988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52196554-C-A

117548988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196554-C-T

117549036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196604-G-A

117549036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196604-G-T

117549038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196606-G-T

117549304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52196999-G-A

117549306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197001-C-G

117549306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197001-C-T

117549394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197069-G-A

117549415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197090-A-G

http://identifiers.org/hco/6/GRCh38#117549443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52197123-C-A

117549443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197123-C-T

117549445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197125-T-C

117549530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197210-G-A

117549530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197210-G-T

117549567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197248-T-C

117549742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197417-T-C

117549762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52197437-G-T

117549813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197488-A-G

http://identifiers.org/hco/6/GRCh38#117549823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52197496-C-A

117549823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197496-C-T

117549835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197508-G-A

117549835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197508-G-T

117549839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52197513-T-C

http://identifiers.org/hco/6/GRCh38#117555729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52207001-C-A

117555825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52207071-T-C

http://identifiers.org/hco/6/GRCh38#117559592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52212359-C-A

117559835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52212581-G-A

117559839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52212585-G-A

117559968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52212693-A-G

117560141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52212857-G-A

117560285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213164-C-T

http://identifiers.org/hco/6/GRCh38#117560422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52213288-C-A

117560422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213288-C-T

117560557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213356-A-G

117560620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213414-G-T

http://identifiers.org/hco/6/GRCh38#117560622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52213416-C-A

117560728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213520-A-T

117560753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213545-G-A

http://identifiers.org/hco/6/GRCh38#117560873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52213603-C-A

117560895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213624-A-G

http://identifiers.org/hco/6/GRCh38#117561010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52213710-C-A

117561010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213710-C-G

117561140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213830-G-C

117561140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213830-G-T

117561251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213904-T-A

117561258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52213910-T-C

http://identifiers.org/hco/6/GRCh38#117561369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52214016-C-A

http://identifiers.org/hco/6/GRCh38#117561393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52214049-C-A

117561444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214100-G-A

117561555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214207-C-T

117561705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214357-T-G

http://identifiers.org/hco/6/GRCh38#117561744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52214396-C-A

117561744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214396-C-T

117562087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214714-A-G

117562100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214727-G-T

117562285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52214922-A-G

117562419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215010-A-G

117562452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215044-C-G

117562452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215044-C-T

117562608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215198-T-G

117562651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215241-A-G

117562740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215330-A-T

117562748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215338-T-A

http://identifiers.org/hco/6/GRCh38#117562811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52215407-C-A

117562811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215407-C-T

117562851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215447-A-T

http://identifiers.org/hco/6/GRCh38#117562875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52215466-C-A

117562979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215561-A-G

http://identifiers.org/hco/6/GRCh38#117563076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52215657-C-A

117563192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215771-T-C

117563225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52215803-T-A

117563959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52216194-G-A

117563959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52216194-G-T

117564332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52216252-T-C

117564506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52216405-A-G

117564575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52216461-C-T

117565254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52220582-C-T

http://identifiers.org/hco/6/GRCh38#117565620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52220914-C-A

117565922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52221156-T-C

117565923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52221157-G-A

117565940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52221174-T-C

117566810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222103-A-G

117566847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 52222138-T-C

http://identifiers.org/hco/6/GRCh38#117566873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52222164-C-A

117566873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52222164-C-T

117567115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222404-G-T

117567125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222414-A-T

117567127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52222416-A-G

117567868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52223729-T-G

117568522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224059-G-A

117568565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224096-C-T

117568742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224266-G-A

117568756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224274-T-C

117568793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224311-A-G

117569085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52224752-C-T

117569450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52225118-A-T

http://identifiers.org/hco/6/GRCh38#117569544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52225140-C-A

117569710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52225306-G-T

http://identifiers.org/hco/6/GRCh38#117569769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52225369-C-A

http://identifiers.org/hco/6/GRCh38#117569838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21479
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#52225436-C-A