153929538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187931-A-G

153929598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187870-T-C

153929608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187860-C-T

153929868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187637-A-G

http://identifiers.org/hco/1/GRCh38#153930008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90187507-C-A

153930008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187507-C-T

153930018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187497-G-A

153930018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187497-G-C

153930043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187472-G-A

153930043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187472-G-T

http://identifiers.org/hco/1/GRCh38#153930045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90187471-A-C

153930045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187471-A-G

http://identifiers.org/hco/1/GRCh38#153930078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90187439-C-A

153930078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187439-C-G

153930078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187439-C-T

http://identifiers.org/hco/1/GRCh38#153930103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90187415-A-C

153930103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187415-A-G

153930115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187403-G-A

153930115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187403-G-C

153930115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90187403-G-T

153930496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90187031-C-T

153930546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90186982-C-T

153930615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186913-G-A

153930618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186910-G-C

153930618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186910-G-T

153930680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186860-G-A

153930719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186821-G-A

153930824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90186716-G-A

153930884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186655-G-T

153930904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186635-T-C

http://identifiers.org/hco/1/GRCh38#153930912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90186627-C-A

153930912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186627-C-G

153930912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186627-C-T

153930964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186574-A-G

153930985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90186553-T-C

153931070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90186468-G-T

153931106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186437-T-C

153931131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186412-C-G

153931131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186412-C-T

153931134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186400-G-A

153931134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186400-G-C

153931170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186340-A-G

153931194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186201-T-C

153931194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90186201-T-G

153932171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90185885-C-T

153932235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185821-A-G

153932499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185552-C-T

http://identifiers.org/hco/1/GRCh38#153932564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90185517-C-A

153932611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185464-G-A

153932630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185445-C-T

153932715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185361-G-A

153932846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185224-C-T

153932856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90185214-G-A

153933025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90185045-C-G

http://identifiers.org/hco/1/GRCh38#153933352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90184693-C-A

153933352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184693-C-T

http://identifiers.org/hco/1/GRCh38#153933366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90184685-A-C

http://identifiers.org/hco/1/GRCh38#153933412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90184641-C-A

153933412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184641-C-T

153933426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184626-T-C

153933432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184620-C-G

153933432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184620-C-T

153933438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184614-A-G

http://identifiers.org/hco/1/GRCh38#153933445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90184607-C-A

153933445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184607-C-G

153933445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90184607-C-T

http://identifiers.org/hco/1/GRCh38#153933505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90184551-C-A

153933505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90184551-C-T

153933798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90184258-C-T

153933858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90184198-C-T

http://identifiers.org/hco/1/GRCh38#153933996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90183835-C-A

http://identifiers.org/hco/1/GRCh38#153934069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90183763-C-A

153934069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90183763-C-T

153934278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90183552-G-T

153934321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90183511-G-A

153934321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90183511-G-T

153934454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90183338-T-G

153934468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90183325-G-A

153934590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90183245-C-T

153934730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90182979-C-G

153934847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90182868-G-T

http://identifiers.org/hco/1/GRCh38#153934973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90182742-C-A

http://identifiers.org/hco/1/GRCh38#153935043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90182691-C-A

153935043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182691-C-T

http://identifiers.org/hco/1/GRCh38#153935116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90182619-C-A

153935116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182619-C-T

http://identifiers.org/hco/1/GRCh38#153935118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90182617-C-A

153935118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182617-C-G

153935118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182617-C-T

153935131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182534-A-G

153935172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182461-G-A

153935172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182461-G-T

153935217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90182396-A-G

http://identifiers.org/hco/1/GRCh38#153935761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90182015-C-A

153935761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90182015-C-T

http://identifiers.org/hco/1/GRCh38#153935813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90181964-C-A

153935813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90181964-C-T

153935998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90181794-G-A

153935998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90181794-G-T

153936015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90181768-A-G

http://identifiers.org/hco/1/GRCh38#153936016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90181767-C-A

153936136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90181646-A-G

http://identifiers.org/hco/1/GRCh38#153936291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90181511-C-A

153936291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90181511-C-T

153936410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90181448-A-T

153936420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90181438-C-T

http://identifiers.org/hco/1/GRCh38#153936433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90181426-C-A

153936509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90181348-C-G

153936509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90181348-C-T

153936603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90181254-A-G

153936663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense variant
orthologous variants: 90181194-C-T

http://identifiers.org/hco/1/GRCh38#153936704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90181153-C-A

153936772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90181085-A-G

153936772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90181085-A-T

153937201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90180860-G-A

153937201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90180860-G-T

153937399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90180438-G-T

http://identifiers.org/hco/1/GRCh38#153937477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90180379-C-A

153937477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90180379-C-T

http://identifiers.org/hco/1/GRCh38#153937478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90180378-C-A

153937479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90180377-A-G

153937480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90180376-C-T

153937878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90180005-T-G

153937915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179966-A-G

153937951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179930-G-A

153937951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179930-G-T

153937979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179895-T-C

153937998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179876-A-G

153938870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179743-G-A

153938890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179723-G-T

153938982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense variant
orthologous variants: 90179624-A-G

153939027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense variant
orthologous variants: 90179579-T-G

153939054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179553-T-G

153939072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179535-G-A

153939072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179535-G-T

http://identifiers.org/hco/1/GRCh38#153939094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90179506-C-A

153939118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179481-T-C

http://identifiers.org/hco/1/GRCh38#153939504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90179181-A-C

153939533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179153-G-A

http://identifiers.org/hco/1/GRCh38#153939552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90179128-C-A

153939552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179128-C-T

153939555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90179125-G-T

153939846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90178831-A-G

http://identifiers.org/hco/1/GRCh38#153939910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90178762-C-A

153939910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90178762-C-T

http://identifiers.org/hco/1/GRCh38#153939962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90178694-C-A

153939962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90178694-C-T

153939983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90178668-T-C

153940074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90178613-C-G

153940104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90178580-G-A

http://identifiers.org/hco/1/GRCh38#153940292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90178404-C-A

http://identifiers.org/hco/1/GRCh38#153940374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90178366-C-A

153940374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90178366-C-T

http://identifiers.org/hco/1/GRCh38#153940402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90178338-C-A

153940402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90178338-C-T

153940705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant
orthologous variants: 90178076-T-C

153940709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90178072-T-C

153940891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant
orthologous variants: 90177909-G-C

http://identifiers.org/hco/1/GRCh38#153940899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90177901-C-A

153940947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90177853-A-G

153941022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90177778-T-C

153941066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90177738-G-A

153941066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90177738-G-T

153941067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90177737-T-C

153941079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90177725-C-T

http://identifiers.org/hco/1/GRCh38#153941136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90177681-C-A

153941172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90177638-C-T

http://identifiers.org/hco/1/GRCh38#153941203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90177607-C-A

153941203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90177607-C-G

http://identifiers.org/hco/1/GRCh38#153941207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90177603-C-A

153941246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90177561-G-A

153941347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90177453-C-T

153941351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90177449-C-G

153941351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90177449-C-T

http://identifiers.org/hco/1/GRCh38#153941467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90177334-C-A

http://identifiers.org/hco/1/GRCh38#153941785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90176858-C-A

153941785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90176858-C-G

153941785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90176858-C-T

153941812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90176832-T-A

153941812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90176832-T-C

153941977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90176675-C-T

153942166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90176483-T-G

http://identifiers.org/hco/1/GRCh38#153942352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90176297-C-A

153942352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90176297-C-G

153942360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90176289-C-G

153942360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90176289-C-T

http://identifiers.org/hco/1/GRCh38#153942603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90176075-C-A

153942657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90176020-A-G

http://identifiers.org/hco/1/GRCh38#153942667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90176010-C-A

153942667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90176010-C-T

153942686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90175992-C-T

153942690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90175988-C-T

http://identifiers.org/hco/1/GRCh38#153942740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90175938-C-A

153942740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90175938-C-T

153942788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90175896-G-A

153942788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90175896-G-C

153943204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90175481-C-G

153943751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90175283-T-A

http://identifiers.org/hco/1/GRCh38#153943949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90175167-C-A

153943949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90175167-C-T

153943954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90175162-T-C

http://identifiers.org/hco/1/GRCh38#153943955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90175161-C-A

153943955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90175161-C-G

153943955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90175161-C-T

153944402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90174713-A-G

153944850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90174267-C-T

http://identifiers.org/hco/1/GRCh38#153945057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90174055-A-C

153945057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90174055-A-G

153945269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90173840-A-G

153945343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90173759-G-T

153945352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90173750-G-A

153945352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron variant
orthologous variants: 90173750-G-T

http://identifiers.org/hco/1/GRCh38#153945913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90173239-C-A

153945913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90173239-C-G

153946199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, undefined
orthologous variants: 90172953-G-A

153946199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: intron_variant, undefined
orthologous variants: 90172953-G-T

153946452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90172717-G-A

153946452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90172717-G-T

153946479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90172698-G-A

153946479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90172698-G-T

153946549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90172626-G-A

153946610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90172565-C-T

http://identifiers.org/hco/1/GRCh38#153946676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90172487-A-C

153946676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29044
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90172487-A-G