156249235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: 88269627-G-T

http://identifiers.org/hco/1/GRCh38#156249481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88269402-C-A

http://identifiers.org/hco/1/GRCh38#156249556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88269331-C-A

156249556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: 88269331-C-T

156249853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: 88269056-C-T

156249858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: 88269050-C-T

156249936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3 prime UTR variant
orthologous variants: 88268992-G-A

156250359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88268642-T-C

156250422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88268578-A-T

156250741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88268277-T-C

156250780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88268244-T-C

156250884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88268171-G-A

156251092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88267972-G-A

156251092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88267972-G-T

156251184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88267872-G-A

156251184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88267872-G-T

156251587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88267536-G-T

156252150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88267162-T-A

http://identifiers.org/hco/1/GRCh38#156252671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88266706-C-A

156252671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88266706-C-T

156252836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88266561-G-A

156252838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88266559-G-A

156252838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88266559-G-C

156252838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88266559-G-T

156253121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266283-T-A

156253121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266283-T-C

156253143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266256-T-G

http://identifiers.org/hco/1/GRCh38#156253198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88266207-C-A

156253257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266155-A-G

156253304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266133-T-A

156253304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266133-T-C

http://identifiers.org/hco/1/GRCh38#156253349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88266090-C-A

156253349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266090-C-T

156253542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265926-G-T

156253581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265900-G-C

156253581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265900-G-T

156253663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265837-G-A

156253663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265837-G-T

156253697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265808-T-C

http://identifiers.org/hco/1/GRCh38#156253698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88265807-C-A

156253698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88265807-C-G

156253807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265718-T-G

156253810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265715-A-G

156253829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265696-T-C

http://identifiers.org/hco/1/GRCh38#156253837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88265692-C-A

156253837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265692-C-G

156253837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265692-C-T

http://identifiers.org/hco/1/GRCh38#156253871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88265658-C-A

156253871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265658-C-T

156254055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88265517-A-G

http://identifiers.org/hco/1/GRCh38#156254238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88265347-A-C

156256585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88264651-A-G

156256764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88264459-G-C

156257922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88263636-A-T

156258983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88263062-G-A

http://identifiers.org/hco/1/GRCh38#156259078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88262968-A-C

156259078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, missense_variant
orthologous variants: 88262968-A-G

156259142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, missense_variant
orthologous variants: 88262904-T-C

http://identifiers.org/hco/1/GRCh38#156259216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88262831-C-A

156259216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262831-C-T

156259292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262769-A-G

156259292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262769-A-T

156259333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262732-T-C

156259936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262350-A-G

http://identifiers.org/hco/1/GRCh38#156260317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88262090-C-A

156260317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262090-C-T

156260327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262080-C-T

156260425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88262036-T-C

http://identifiers.org/hco/1/GRCh38#156260443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88262020-A-C

156260482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88261981-G-A

http://identifiers.org/hco/1/GRCh38#156260560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88261903-C-A

http://identifiers.org/hco/1/GRCh38#156260646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88261819-A-C

156260646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261819-A-G

156260730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261754-G-A

156260730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261754-G-C

156260730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261754-G-T

http://identifiers.org/hco/1/GRCh38#156260740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88261743-A-C

156260740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261743-A-G

156260740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261743-A-T

http://identifiers.org/hco/1/GRCh38#156260809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88261691-C-A

156260863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261638-G-T

156261281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261299-T-C

156261286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261294-A-T

156261322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88261267-G-A

156261414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88261175-G-A

156262913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260844-C-T

156262929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260828-T-C

156263012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260750-T-A

156263052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260716-T-C

156263093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260675-T-C

156263576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88260264-G-A

156263576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88260264-G-C

156263580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260260-G-A

156263596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260246-A-T

156263600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260242-A-T

http://identifiers.org/hco/1/GRCh38#156263653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88260197-C-A

156263653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260197-C-T

156263690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260162-G-A

156263690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260162-G-T

156263706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260154-G-A

156263706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260154-G-T

http://identifiers.org/hco/1/GRCh38#156263722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88260136-C-A

156263722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88260136-C-T

156265544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88259034-G-C

156265689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88258926-G-T

http://identifiers.org/hco/1/GRCh38#156266002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88258665-C-A

156266002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88258665-C-T

156266116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88258551-G-A

156266140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88258527-T-C

156266174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88258493-G-A

156266174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88258493-G-C

156266311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88258350-G-A

http://identifiers.org/hco/1/GRCh38#156266588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88258092-A-C

156267150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257692-C-T

156267529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88257470-A-T

156267590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88257409-G-A

156267590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88257409-G-C

156267697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88257302-A-G

156267702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88257297-G-A

156268077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88256779-T-C

156268203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88256661-A-G

156268241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88256623-A-G

http://identifiers.org/hco/1/GRCh38#156268581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88256234-C-A

156268581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88256234-C-T

156268611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88256204-G-A

156272176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255243-T-A

156272176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255243-T-C

156272192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255227-G-T

http://identifiers.org/hco/1/GRCh38#156272232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88255108-A-C

156272232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255108-A-T

156272233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255107-G-A

156272233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255107-G-C

156272243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255097-G-A

156272243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88255097-G-T

http://identifiers.org/hco/1/GRCh38#156272450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88254786-C-A

156272450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254786-C-T

156272487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254772-G-A

156272487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254772-G-C

156272487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254772-G-T

156272488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254771-T-C

156272488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254771-T-G

156272641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254630-C-T

156272807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254511-G-A

156272940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88254314-T-C

156273277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88253916-T-G

156273289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88253906-G-A

156273289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88253906-G-T

156274202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88253273-C-T

156274406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252905-C-T

http://identifiers.org/hco/1/GRCh38#156274511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88252843-C-A

156274511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252843-C-T

156274638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88252716-T-C

http://identifiers.org/hco/1/GRCh38#156274723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88252621-C-A

156274810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252537-G-A

156274810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252537-G-C

156274810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252537-G-T

156275020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252388-A-G

156275196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88252162-G-A

156276145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88251213-G-T

156276157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88251198-C-T

http://identifiers.org/hco/1/GRCh38#156276166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88251189-A-C

156276166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88251189-A-G

156276166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88251189-A-T

156276417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250982-G-A

156276417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250982-G-C

http://identifiers.org/hco/1/GRCh38#156276614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88250741-C-A

156276820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250554-C-T

156277020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250380-G-A

156277020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250380-G-T

156277311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250127-T-A

156277311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250127-T-C

156277311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250127-T-G

156277322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88250100-C-T

156277995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: missense variant
orthologous variants: 88249799-C-T

156278043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 88249751-C-G

156278043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 88249751-C-T

156278092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249705-G-A

156278092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249705-G-C

156278092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249705-G-T

156278112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249684-A-G

156278126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249673-T-C

156278126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249673-T-G

156278804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249382-G-A

156278804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88249382-G-T

156279641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88248530-T-C

156279654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88248517-A-G

156280173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88246807-G-T

156280193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88246787-G-T

156280479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88246506-T-C

156280521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88246443-T-C

http://identifiers.org/hco/1/GRCh38#156280675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88246142-C-A

156280853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88245698-T-C

156280914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88245659-C-T

156281352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88245151-T-C

156281353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88245150-T-C

156281676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88244892-A-T

156281686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88244882-T-C

156281741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88244822-C-T

156281756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88244807-T-G

156281769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron variant
orthologous variants: 88244794-G-C

156282531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88243876-C-G

156282531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88243876-C-T

http://identifiers.org/hco/1/GRCh38#156282693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88243716-C-A

156282693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88243716-C-T

156282735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88243674-C-T

156282759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88243650-G-A

156282876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88243533-A-G

http://identifiers.org/hco/1/GRCh38#156282878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88243531-C-A

156282878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88243531-C-G

156282878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88243531-C-T

156282931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, undefined
orthologous variants: 88243478-T-A

156282941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243468-A-G

156282986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243427-G-A

156283016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243397-A-G

156283018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243395-G-A

156283018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243395-G-C

156283018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243395-G-T

http://identifiers.org/hco/1/GRCh38#156283028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88243385-C-A

156283028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88243385-C-T

http://identifiers.org/hco/1/GRCh38#156283041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88243372-C-A

156283041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243372-C-T

156283053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243363-T-A

156283053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243363-T-C

156283053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88243363-T-G

156283076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88243339-A-G

156283233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88243127-T-A

156283234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88243126-G-A

http://identifiers.org/hco/1/GRCh38#156283279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88243074-C-A

156283279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88243074-C-T

156283309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88243013-C-T

156284017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88242048-A-G

156284084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88241986-C-T

156284255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88241817-G-A

156285689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24644
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88240491-G-A