http://identifiers.org/hco/17/GRCh38#4499114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72380553-C-A

4499114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380553-C-G

4499114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380553-C-T

4499177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380490-G-A

4499177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380490-G-T

http://identifiers.org/hco/17/GRCh38#4499372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72380295-A-C

4499372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380295-A-G

4499394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72380273-A-G

4499394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72380273-A-T

http://identifiers.org/hco/17/GRCh38#4499434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72380233-C-A

4499434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380233-C-T

4499584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380116-T-C

4499632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380072-G-A

4499632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72380072-G-T

http://identifiers.org/hco/17/GRCh38#4499685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72380018-C-A

4499685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380018-C-T

http://identifiers.org/hco/17/GRCh38#4499755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72379952-C-A

4499755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379952-C-G

4499755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379952-C-T

4499765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379942-G-A

4499765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379942-G-T

http://identifiers.org/hco/17/GRCh38#4499784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72379923-C-A

4499784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379923-C-G

4499784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379923-C-T

http://identifiers.org/hco/17/GRCh38#4499810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72379900-A-C

4499810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379900-A-G

4499826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379884-C-T

4499993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379705-G-A

4499993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379705-G-T

4500018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379680-G-A

4500018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379680-G-T

4500047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379651-G-A

4500069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379629-G-A

http://identifiers.org/hco/17/GRCh38#4500655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72379077-C-A

4500799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72378934-C-T

4500838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72378896-G-T

4500967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72378771-T-A

4501276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72378465-C-T

http://identifiers.org/hco/17/GRCh38#4501575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72378208-C-A

4501835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377961-T-C

4502521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377141-G-A

4502553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377108-C-T

4502569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377092-C-G

4502569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377092-C-T

http://identifiers.org/hco/17/GRCh38#4502848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72376845-C-A

4502895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376795-A-G

4502942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376737-C-T

http://identifiers.org/hco/17/GRCh38#4502986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72376695-C-A

4503037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376649-C-T

4503678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376336-G-A

4504038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375993-A-G

4504340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375748-A-G

4504399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375690-G-A

4504399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375690-G-T

4504518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375588-G-C

4504649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375432-G-A

4504846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375154-C-G

4505012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72374926-G-A

4505404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72373756-G-A

4505469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72373691-A-G

4505648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72373514-G-A

4505800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72373416-G-T

4506810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72372563-C-G

4507091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72372371-C-T

4507361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72372125-T-C

http://identifiers.org/hco/17/GRCh38#4507367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72372119-A-C

4507397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72372104-C-T

4507709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72371815-C-T

4508164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72371342-G-A

4508242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72371275-C-G

4508242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72371275-C-T

http://identifiers.org/hco/17/GRCh38#4508423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72370797-C-A

4509138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72370179-T-C

4509155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72370164-G-A

4509597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72369686-G-T

4509667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72369638-T-C

http://identifiers.org/hco/17/GRCh38#4509699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72369611-C-A

4509699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72369611-C-G

4509839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72369446-T-A

4510032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72369237-G-A

4510196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72369090-G-A

4510281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72369035-G-A

4510459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72368904-C-T

4510620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72368807-C-T

4510936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367717-A-G

http://identifiers.org/hco/17/GRCh38#4510937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72367716-C-A

4511475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367194-A-G

4511771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366851-C-G

4511796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366827-C-T

4511849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366773-G-A

http://identifiers.org/hco/17/GRCh38#4511873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72366750-C-A

4512134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366540-G-C

4512726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366071-G-A

4512873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365962-G-A

http://identifiers.org/hco/17/GRCh38#4513119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72365713-C-A

4513119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365713-C-G

4513119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365713-C-T

4513294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72365547-G-A

http://identifiers.org/hco/17/GRCh38#4513328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72365514-C-A

4513328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365514-C-T

4513410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365454-G-A

4513410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365454-G-T

http://identifiers.org/hco/17/GRCh38#4513417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72365447-C-A

4513417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365447-C-G

4513417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365447-C-T

4513438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365423-T-A

http://identifiers.org/hco/17/GRCh38#4513453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72365408-A-C

4513453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365408-A-G

http://identifiers.org/hco/17/GRCh38#4513487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72365375-A-C

4513936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364964-C-T

4514127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364769-C-T

4514796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364184-C-G

4515189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363874-T-C

http://identifiers.org/hco/17/GRCh38#4515243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72363819-C-A

4515243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363819-C-T

http://identifiers.org/hco/17/GRCh38#4515520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72363605-A-C

4515941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363244-A-G

4515941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363244-A-T

4516604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72362966-C-T

4516906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72362658-G-A

http://identifiers.org/hco/17/GRCh38#4516952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72362619-C-A

4517010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72362567-T-C

4520429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359525-T-A

4520490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359482-G-A

http://identifiers.org/hco/17/GRCh38#4520543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72359446-C-A

4520715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359302-G-A

4521394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72358133-G-A

4521428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72358099-G-A

http://identifiers.org/hco/17/GRCh38#4521487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72358047-A-C

4521487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72358047-A-G

4521545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357985-C-T

4521925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357625-A-G

4522365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357487-G-A

4522727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357239-C-T

4524090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355728-G-C

4524168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355644-C-T

4524557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355143-G-A

4524559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355141-C-G

4524712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354967-A-T

4524928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354719-G-T

http://identifiers.org/hco/17/GRCh38#4524948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72354698-C-A

4524986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354647-C-T

4525223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354424-C-G

4525223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354424-C-T

4525247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354396-G-A

4525247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354396-G-C

4525302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354376-G-A

4525302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354376-G-T

4525499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354177-C-T

4525576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354103-C-T

4525742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353938-A-T

4525772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353908-T-C

4525778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353902-G-A

4525855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353829-G-A

4525878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353806-C-G

4525912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353771-G-C

4526096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353625-G-A

4526103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353618-G-C

4526910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353253-C-G

4527184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353014-A-G

4527326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352876-G-A

4527515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352684-C-G

4527627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352572-C-T

4527652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352549-T-G

4527783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352425-C-T

4529929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350473-G-A

4529929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350473-G-C

4530249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350187-G-A

4530446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350049-A-T

4530532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349972-G-A

4530532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349972-G-T

4530555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349949-G-A

4530574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349933-G-T

4530596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349913-A-G

http://identifiers.org/hco/17/GRCh38#4530741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72349768-C-A

4530741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72349768-C-T

4530817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349694-A-G

4530828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349685-G-A

4530828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349685-G-C

4530828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349685-G-T

4530908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349641-G-A

4530908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349641-G-C

4530908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349641-G-T

4530919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349630-G-T

http://identifiers.org/hco/17/GRCh38#4530934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72349616-C-A

http://identifiers.org/hco/17/GRCh38#4530941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72349609-C-A

4530941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349609-C-T

http://identifiers.org/hco/17/GRCh38#4530953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72349597-C-A

4530953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349597-C-T

4530961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349589-G-A

4531015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349565-T-C

4531216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349370-A-G

4531237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349349-T-C

4531345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349272-G-T

4531578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349040-A-G

4532322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72348375-G-C

4532384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72348312-A-G

4532431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72348260-A-G

4532740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347981-G-A

http://identifiers.org/hco/17/GRCh38#4532785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347961-C-A

4532785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347961-C-G

4532785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347961-C-T

http://identifiers.org/hco/17/GRCh38#4532786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347960-C-A

4532786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347960-C-G

http://identifiers.org/hco/17/GRCh38#4532799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347947-C-A

4532799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347947-C-G

http://identifiers.org/hco/17/GRCh38#4532842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347905-C-A

4532842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347905-C-T

http://identifiers.org/hco/17/GRCh38#4532853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347894-A-C

http://identifiers.org/hco/17/GRCh38#4532860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347887-C-A

4532860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347887-C-T

4532985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72347743-A-T

4533172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347567-G-A

4533172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347567-G-C

4533172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347567-G-T

http://identifiers.org/hco/17/GRCh38#4533189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347561-A-C

4533189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347561-A-G

http://identifiers.org/hco/17/GRCh38#4533226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347530-A-C

4533226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347530-A-G

4533298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72347458-G-A

4533298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72347458-G-T

4533334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72347422-C-T

4533440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72347316-C-G

4533440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72347316-C-T

4533441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347315-A-G

4533441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347315-A-T

4533518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347271-T-C

4533518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347271-T-G

4533860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72347120-C-G

4533860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72347120-C-T

4533872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347108-G-A

4533880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347100-T-G

http://identifiers.org/hco/17/GRCh38#4533911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347068-A-C

4533911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347068-A-G

4533911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347068-A-T

4533923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347056-G-A

4533923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347056-G-T

http://identifiers.org/hco/17/GRCh38#4533929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72347050-C-A

4533929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347050-C-G

4533929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347050-C-T

4533998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346993-G-A

4533998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346993-G-T

4533999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346992-G-A

4533999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346992-G-C

4533999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346992-G-T

4534081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346925-G-T

4534263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72346720-G-A

4534263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72346720-G-T

4534276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72346707-G-A

4534424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72346550-G-T

4534555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346434-G-A

4534555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346434-G-T

4534563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346424-G-C

4534563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346424-G-T

4534635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346361-A-G

4534767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346234-A-G

4534775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346226-G-A

4534797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346216-G-C

4534804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346209-C-T

4534831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346182-G-A

4534835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346178-A-G

4534908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346103-G-C

4534908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346103-G-T

4534990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346011-C-T

4535051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345958-C-T

4535181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345861-T-A

4535181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345861-T-C

4535223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345844-T-G

4535298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345787-C-G

4535298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345787-C-T

4535312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345772-G-A

4535475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345597-C-G

http://identifiers.org/hco/17/GRCh38#4535479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72345593-A-C

4535618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345477-G-A

4535652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345454-A-G

4535709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345398-T-G

4535993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345297-T-A

4535993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345297-T-C

4535993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345297-T-G

4535994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345296-T-C

4536347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344957-T-C

4536473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344841-G-A

4536473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344841-G-C

4536473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344841-G-T

http://identifiers.org/hco/17/GRCh38#4536474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72344840-A-C

4536474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344840-A-G

4536556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344774-T-A

4536604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344731-T-A

4536604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344731-T-C

4536604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344731-T-G

4536635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344697-G-A

4536635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344697-G-T

4536664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72344664-T-C

4537292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344076-T-A

4537327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344042-A-G

4537328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344041-G-A

4537328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344041-G-C

4537328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344041-G-T

http://identifiers.org/hco/17/GRCh38#4537371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72344014-A-C

4537371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344014-A-G

4537371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344014-A-T

http://identifiers.org/hco/17/GRCh38#4537380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72344005-A-C

4537380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344005-A-G

4537380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344005-A-T

4537397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343991-A-G

4537397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343991-A-T

http://identifiers.org/hco/17/GRCh38#4537407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343981-C-A

4537407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343981-C-T

http://identifiers.org/hco/17/GRCh38#4537481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343917-C-A

4537481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343917-C-G

http://identifiers.org/hco/17/GRCh38#4537568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343830-C-A

4537568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343830-C-T

4537581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343817-C-T

http://identifiers.org/hco/17/GRCh38#4537586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343812-C-A

4537586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343812-C-T

4537726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72343675-G-A

4537733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343668-G-A

4537733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343668-G-T

4537736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343665-G-A

4537736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72343665-G-C

http://identifiers.org/hco/17/GRCh38#4537770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343631-A-C

4537810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343588-G-A

4537810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343588-G-C

4538009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343390-G-A

http://identifiers.org/hco/17/GRCh38#4538041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343360-C-A

4538041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343360-C-T

http://identifiers.org/hco/17/GRCh38#4538050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343351-C-A

4538050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343351-C-T

http://identifiers.org/hco/17/GRCh38#4538064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343323-C-A

4538064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343323-C-T

4538130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343250-G-A

http://identifiers.org/hco/17/GRCh38#4538179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343194-C-A

http://identifiers.org/hco/17/GRCh38#4538240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343178-C-A

4538240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343178-C-T

http://identifiers.org/hco/17/GRCh38#4538249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72343169-C-A

4538249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343169-C-G

4538249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343169-C-T

4538334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343114-G-A

4538334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343114-G-T

4538444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343024-C-G

4538444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72343024-C-T

4538475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342991-G-C

4538475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342991-G-T

4538486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342972-T-C

4538486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342972-T-G

http://identifiers.org/hco/17/GRCh38#4538502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72342956-C-A

4538502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342956-C-T

http://identifiers.org/hco/17/GRCh38#4538540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72342932-C-A

4538540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342932-C-G

4538540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342932-C-T

4538651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342841-T-A

4538651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342841-T-C

4538709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72342786-A-G

4538969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26992
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72342531-T-C