55228245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4632609-C-T

55228526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4632997-C-T

55228560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4633029-G-A

55228807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4633322-G-C

http://identifiers.org/hco/19/GRCh38#55230021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4634695-C-A

55230021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634695-C-T

55230084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634745-T-A

55230084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634745-T-C

http://identifiers.org/hco/19/GRCh38#55230146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4634783-C-A

http://identifiers.org/hco/19/GRCh38#55230170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4634807-C-A

55230170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634807-C-T

55230176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634812-A-G

http://identifiers.org/hco/19/GRCh38#55230181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4634817-A-C

55230181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634817-A-G

55230232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634866-C-T

55230278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4634984-T-C

55230440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4635155-T-C

http://identifiers.org/hco/19/GRCh38#55230597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4635324-C-A

55230597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635324-C-T

http://identifiers.org/hco/19/GRCh38#55230731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4635442-C-A

55230731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635442-C-T

http://identifiers.org/hco/19/GRCh38#55230745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4635459-C-A

55230745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635459-C-G

55230745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635459-C-T

http://identifiers.org/hco/19/GRCh38#55230816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4635530-C-A

55230816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4635530-C-T

http://identifiers.org/hco/19/GRCh38#55230999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4635682-C-A

55231004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635687-G-A

55231004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635687-G-C

55231020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635703-G-A

55231020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635703-G-T

http://identifiers.org/hco/19/GRCh38#55231091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4635770-C-A

55231091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635770-C-G

55231091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635770-C-T

55231269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635933-G-A

55231269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635933-G-T

55231318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635970-G-T

55231346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635993-C-G

55231346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4635993-C-T

55231382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4636030-T-A

55231382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4636030-T-C

http://identifiers.org/hco/19/GRCh38#55231702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636375-C-A

55231817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4636483-T-C

http://identifiers.org/hco/19/GRCh38#55232021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636640-C-A

55232043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4636660-T-A

55232047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4636664-C-T

55232072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4636690-C-T

55232079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636697-A-G

55232079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636697-A-T

55232101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4636719-T-C

55232101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4636719-T-G

http://identifiers.org/hco/19/GRCh38#55232117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636735-C-A

55232117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4636735-C-G

55232117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4636735-C-T

55232136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636754-G-A

55232136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636754-G-C

55232136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636754-G-T

http://identifiers.org/hco/19/GRCh38#55232148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636763-C-A

55232148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636763-C-T

55232151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636766-G-A

55232151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4636766-G-T

http://identifiers.org/hco/19/GRCh38#55232163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636778-C-A

55232163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636778-C-T

55232178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4636790-T-C

55232260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4636867-G-A

55232260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4636867-G-C

http://identifiers.org/hco/19/GRCh38#55232265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636873-C-A

55232265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4636873-C-T

55232306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4636889-G-A

55232306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4636889-G-C

http://identifiers.org/hco/19/GRCh38#55232338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4636923-C-A

http://identifiers.org/hco/19/GRCh38#55236274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4638599-C-A

55236274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4638599-C-T

http://identifiers.org/hco/19/GRCh38#55236313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4638637-C-A

55236313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4638637-C-T

55236316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4638640-A-G

55236316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4638640-A-T

55236575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4638868-G-A

http://identifiers.org/hco/19/GRCh38#55236627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4638948-C-A

55236633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4638954-G-A

55236633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4638954-G-T

55236998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4639288-A-G

55236998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4639288-A-T

55237061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4639340-A-T

55237066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4639344-A-T

55239158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4641390-T-C

55239158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4641390-T-G

55239340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4642451-C-G

55239388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4642496-G-A

55239388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4642496-G-T

http://identifiers.org/hco/19/GRCh38#55239514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4642624-C-A

55239514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4642624-C-T

55239645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4642741-C-T

55239672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4642768-G-A

55239856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4642922-C-T

55239917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 4642983-T-C

55239930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4642995-T-C

55239952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4643012-G-A

55239956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4643016-C-G

55239956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4643016-C-T

55239982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4643057-G-A

55239982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4643057-G-T

55239986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4643061-T-C

55240003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4643076-C-T

55240135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4643209-G-A

http://identifiers.org/hco/19/GRCh38#55240191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4643265-A-C

55240226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4643298-A-G

55240226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4643298-A-T

55240268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4643340-G-A

55240268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4643340-G-T

55240338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4643406-T-C

55240726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4643867-T-A

55240726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4643867-T-C

http://identifiers.org/hco/19/GRCh38#55240754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4643895-C-A

55241204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644241-G-C

55241204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644241-G-T

http://identifiers.org/hco/19/GRCh38#55241278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4644303-C-A

55241278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4644303-C-G

55241278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4644303-C-T

55241298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4644323-C-T

55241457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644484-C-T

55241668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644697-T-A

55241724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644720-G-A

55241724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644720-G-C

55241724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644720-G-T

55242024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644833-A-T

http://identifiers.org/hco/19/GRCh38#55242100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4644866-C-A

55242100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4644866-C-T

55242284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4645045-G-A

55242284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4645045-G-C

55242284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4645045-G-T

55242314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4645069-C-T

55242357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4645114-G-A

55242357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4645114-G-T

55242464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4645223-G-A

55242464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4645223-G-C

55242503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4645261-G-A

55242503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4645261-G-C

55242560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4645301-C-G

55242590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4645321-T-C

55245044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4645927-C-T

55245049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4645934-T-C

55245083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4645953-T-A

55245083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4645953-T-C

55245211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4646099-A-G

55245298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4646181-C-T

55245307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4646190-G-A

55245322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4646205-G-A

55245445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4646328-C-T

55245700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4646577-G-A

55245700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4646577-G-T

http://identifiers.org/hco/19/GRCh38#55245794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4646645-C-A

55245794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4646645-C-T

http://identifiers.org/hco/19/GRCh38#55246972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4649802-C-A

55246972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4649802-C-G

55246972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4649802-C-T

55246986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense variant
orthologous variants: 4649816-C-G

55246986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense variant
orthologous variants: 4649816-C-T

55247014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense variant
orthologous variants: 4649844-C-G

55247017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: synonymous variant
orthologous variants: 4649847-G-A

55247017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: missense variant
orthologous variants: 4649847-G-C

55247189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4650006-G-A

55247189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4650006-G-C

55247189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4650006-G-T

55247267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4650067-G-A

55247267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4650067-G-T

http://identifiers.org/hco/19/GRCh38#55247291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4650098-A-C

http://identifiers.org/hco/19/GRCh38#55247364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4650133-C-A

55247388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650157-A-G

55247400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650169-T-C

55247403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650172-T-C

55247416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650186-G-T

55247428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650198-G-A

http://identifiers.org/hco/19/GRCh38#55247449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4650218-C-A

55247449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650218-C-G

55247449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650218-C-T

55247470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650237-G-A

55247810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4650554-G-C

http://identifiers.org/hco/19/GRCh38#55248315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4650947-A-C

55251535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4654522-T-C

55251887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4654816-A-G

55251907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4654836-G-A

55253059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4655510-C-T

http://identifiers.org/hco/19/GRCh38#55253129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4656302-A-C

55254120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4656883-T-C

55254204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4656961-C-T

55254538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4657299-C-T

55254941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4657679-G-C

55255654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4658455-A-G

55255717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4658533-C-T

http://identifiers.org/hco/19/GRCh38#55255725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4658541-C-A

55255725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4658541-C-T

http://identifiers.org/hco/19/GRCh38#55255745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4658558-C-A

55255745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4658558-C-T

http://identifiers.org/hco/19/GRCh38#55255828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4658641-C-A

55255828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4658641-C-T

55255913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4658691-G-T

55256096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4659092-C-G

http://identifiers.org/hco/19/GRCh38#55256381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4659374-C-A

55257473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4660483-G-A

55257473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4660483-G-T

55257478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4660488-C-G

55257878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4660876-G-A

55258191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4661201-G-C

55258262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4661280-G-A

55258293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4661305-A-G

55258330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4661336-G-A

55258330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4661336-G-T

55258347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron variant
orthologous variants: 4661353-A-G

http://identifiers.org/hco/19/GRCh38#55258428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4661473-C-A

http://identifiers.org/hco/19/GRCh38#55258631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4661686-C-A

55258631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661686-C-T

55258649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661701-T-C

55258649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661701-T-G

55258784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661776-C-T

55258821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661813-A-G

55258882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661871-A-G

http://identifiers.org/hco/19/GRCh38#55258908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4661888-C-A

55258908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661888-C-T

http://identifiers.org/hco/19/GRCh38#55258964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4661947-C-A

55258964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661947-C-T

55258983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661966-C-G

55258983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661966-C-T

55258987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661970-G-A

55258987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29195
most severe consequence: 5 prime UTR variant
orthologous variants: 4661970-G-T