157257728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888047-G-A

157257728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888047-G-T

157257788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888101-C-T

157257878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888190-G-A

157257878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888190-G-T

157257940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888258-T-G

157257954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888272-G-A

157257954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888272-G-T

157257961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888279-G-A

157257961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888279-G-T

157257963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888281-G-A

157257963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888281-G-T

157257971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888289-T-C

157257971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888289-T-G

157257977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888294-T-A

157257977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888294-T-C

157258008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888334-C-T

http://identifiers.org/hco/2/GRCh38#157258014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57888340-C-A

157258014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57888340-C-T

157258212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57888531-G-A

157258212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57888531-G-T

157258327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57888634-G-A

http://identifiers.org/hco/2/GRCh38#157258336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#57888643-C-A

157258336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57888643-C-T

157258427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57888734-G-A

157258478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57888785-G-A

157258517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57888824-C-T

157258570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57888877-C-G

157258570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57888877-C-T

157258744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889051-G-C

157258769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57889076-G-A

157258769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889076-G-C

157258770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 57889077-C-T

157258824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889131-A-G

157258836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889143-G-A

157258869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889176-A-G

157258906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889204-G-T

http://identifiers.org/hco/2/GRCh38#157258931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#57889229-C-A

http://identifiers.org/hco/2/GRCh38#157258972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57889270-C-A

157259012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57889310-T-C

157259179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889477-T-A

157259179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889477-T-C

157259206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889504-G-C

http://identifiers.org/hco/2/GRCh38#157259282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57889577-C-A

157259282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57889577-C-T

157259371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57889660-T-C

157259611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57889893-T-C

http://identifiers.org/hco/2/GRCh38#157259632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57889914-C-A

157259676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57889959-A-G

157259767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57890182-T-C

157259923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57890425-G-A

157259923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57890425-G-C

http://identifiers.org/hco/2/GRCh38#157260633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57890975-C-A

157260751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57891094-G-A

157260751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57891094-G-C

157260964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57891304-A-G

157261216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57891549-G-A

157261317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57891637-G-A

157261340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57891660-T-C

157261663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57891987-C-T

157261697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57892022-C-G

157262178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57892461-C-T

http://identifiers.org/hco/2/GRCh38#157262197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#57892477-C-A

157262197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57892477-C-T

157262205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57892485-T-A

157262205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57892485-T-C

157262205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57892485-T-G

http://identifiers.org/hco/2/GRCh38#157262790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57892723-C-A

157263403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57893371-T-A

157263403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57893371-T-C

157263551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57893510-G-A

157263551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57893510-G-C

157263668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57893624-C-T

157263908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57893863-T-G

157264935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57895137-C-T

157265100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57895292-A-G

157265131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57895317-G-A

157265533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57895811-G-A

157265763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57896056-G-A

157266192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57896467-T-C

157266648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57896863-G-A

157266763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57896950-G-A

157266777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57896964-T-A

157266854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 57897041-T-C

157267604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57897226-C-T

157267724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57897345-T-C

157268275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57897881-C-G

157268285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57897891-G-A

157268343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57897947-C-T

157268429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57898031-C-T

http://identifiers.org/hco/2/GRCh38#157268454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57898054-C-A

http://identifiers.org/hco/2/GRCh38#157268492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57898093-C-A

157268561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57898162-G-A

157268642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57898240-G-A

157268973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57898566-T-C

157273161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57899397-T-C

157273346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57899561-T-C

157273519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57899729-G-A

http://identifiers.org/hco/2/GRCh38#157273582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57899803-A-C

157275356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57901670-A-G

157281744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57902587-T-A

157281878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57902697-A-T

157281930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57902748-T-C

157281931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57902749-G-A

157281931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57902749-G-T

157282790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903536-T-G

157282815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903562-T-C

http://identifiers.org/hco/2/GRCh38#157282880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57903650-A-C

157283071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903837-T-C

157283090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903852-A-G

http://identifiers.org/hco/2/GRCh38#157283164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57903926-A-C

157283164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903926-A-T

157283171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903932-T-C

157283246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57903999-T-C

157283413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904169-G-A

157283413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904169-G-T

157283418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904174-T-C

157283565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904320-A-G

157283703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904490-A-G

157283738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904521-G-A

157284190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904788-G-A

157284190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904788-G-C

157284190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904788-G-T

http://identifiers.org/hco/2/GRCh38#157284202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57904800-C-A

157284202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57904800-C-T

157284382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57904963-G-A

157284581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57905153-T-A

157284783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57905438-C-T

157285175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57905967-T-A

157285296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57906083-T-G

157285463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57906356-C-T

157285492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57906400-T-C

157285841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57906977-G-C

157285858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57906994-A-G

http://identifiers.org/hco/2/GRCh38#157285951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57907083-C-A

157285951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907083-C-G

157285951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907083-C-T

157286075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57907190-G-A

157286075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57907190-G-T

157286143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907258-T-C

157286187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907309-G-A

157286188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907310-T-C

157286303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907415-T-C

157286305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907417-G-A

157286307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57907419-C-T

157287313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57908337-G-C

157287321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57908359-A-G

http://identifiers.org/hco/2/GRCh38#157287382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57908432-C-A

157288076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57908633-C-T

157288209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57908745-G-A

157288602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57910414-G-A

157288812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57910598-T-C

157288869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57910653-A-T

157288915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57910699-G-A

157289126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57910928-T-G

157289143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57910945-G-A

157289489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57911271-C-T

http://identifiers.org/hco/2/GRCh38#157289579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57911337-A-C

157289591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57911349-C-T

http://identifiers.org/hco/2/GRCh38#157289593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57911351-C-A

157289748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57911496-T-C

157289767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57911520-T-C

http://identifiers.org/hco/2/GRCh38#157290073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57911739-C-A

157290322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912007-G-A

157290343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912031-C-T

157290344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912032-G-A

157290388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912068-C-G

157290639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912312-A-G

157291325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57912811-C-T

157291334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57912820-T-A

157291337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912823-A-G

157291509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57912975-A-G

157291588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57913054-G-A

157295440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914379-T-G

157295446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914385-A-G

157295554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914489-T-A

157295554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914489-T-G

157295602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914537-G-A

157295602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914537-G-T

157295623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914558-T-C

157295894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914799-A-G

157295903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914808-G-A

157295903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914808-G-T

http://identifiers.org/hco/2/GRCh38#157295940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57914843-C-A

157295940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57914843-C-T

157296283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57915156-A-T

157296342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57915225-T-A

157296342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57915225-T-C

157296517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57915416-A-T

http://identifiers.org/hco/2/GRCh38#157296655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57915548-C-A

157299295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57915815-T-C

157299361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57915880-G-T

http://identifiers.org/hco/2/GRCh38#157299392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57915909-C-A

http://identifiers.org/hco/2/GRCh38#157299478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57915988-C-A

http://identifiers.org/hco/2/GRCh38#157299511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57916021-A-C

157299511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916021-A-G

157299611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57916119-A-G

157299706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916491-G-A

157299718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916503-T-A

157299772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916557-A-G

157299772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916557-A-T

157299779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916564-A-G

157299792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916576-T-C

157299825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916607-A-G

157300079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916872-C-T

157300091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916884-G-T

157300100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916888-A-G

157300153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916943-A-G

157300207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57916987-G-C

http://identifiers.org/hco/2/GRCh38#157300343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57917106-C-A

157300408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917566-G-A

157300580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917744-G-A

157300597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917769-T-G

157300600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917772-T-C

157300607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917779-T-C

157300638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917810-T-G

157300651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57917823-G-C

157300771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57917944-G-A

157300882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57918055-T-C

157300981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57918154-T-C

http://identifiers.org/hco/2/GRCh38#157301104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918252-C-A

157301109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918257-A-G

157301132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918280-T-A

157301162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918309-G-C

157301283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918405-T-C

http://identifiers.org/hco/2/GRCh38#157301356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918471-A-C

157301356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918471-A-T

http://identifiers.org/hco/2/GRCh38#157301358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918473-A-C

157301358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918473-A-G

157301362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918477-G-A

157301362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918477-G-T

http://identifiers.org/hco/2/GRCh38#157301378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918492-C-A

157301378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918492-C-G

157301378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918492-C-T

http://identifiers.org/hco/2/GRCh38#157301382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918496-C-A

157301382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918496-C-G

157301382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918496-C-T

http://identifiers.org/hco/2/GRCh38#157301386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918500-A-C

157301386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918500-A-G

http://identifiers.org/hco/2/GRCh38#157301397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57918511-C-A

157301397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918511-C-G

157301397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918511-C-T

157301498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918602-A-G

157301498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918602-A-T

157301570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918662-G-A

157301570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918662-G-T

157301593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918688-G-A

157301593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57918688-G-T

157301728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57918771-G-T

157301773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57918816-T-C

157301921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57918941-C-T

157302062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57919048-T-C

157302084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57919071-T-G

157302128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57919094-C-T

http://identifiers.org/hco/2/GRCh38#157302340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57919299-A-C

157302451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57919403-T-C

157302499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57919443-G-T

http://identifiers.org/hco/2/GRCh38#157302665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57919567-C-A

157302665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57919567-C-T

157302794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57919688-T-C

157303404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57920095-T-C

157303428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57920119-G-A

157303951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57920431-C-T

157304150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57920598-A-T

157304230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57920651-C-G

157304253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57920674-A-T

157304383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57920800-T-C

157304456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57920869-G-C

http://identifiers.org/hco/2/GRCh38#157304511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57920920-C-A

157304746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921161-C-T

157304851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921269-A-G

157304921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921307-A-G

157305051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921412-T-A

157305052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921413-C-T

157305115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921466-G-C

157305395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921759-T-C

157305558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57921923-G-A

157305717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922087-T-C

157305858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922231-T-A

http://identifiers.org/hco/2/GRCh38#157305861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57922234-C-A

157305862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922235-T-C

http://identifiers.org/hco/2/GRCh38#157305892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57922266-C-A

157306111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922485-T-G

157306112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922486-G-A

157306186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922542-C-G

157306217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922573-T-C

157306238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922596-T-A

157306238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922596-T-C

157306251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922614-T-C

157306385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922931-C-T

157306387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922933-A-G

157306400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922946-G-C

157306407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922959-C-T

157306408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57922960-T-C

157306506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923057-C-T

157306525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923076-C-T

157306563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923100-G-T

157306675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923205-A-G

157306919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923439-A-G

http://identifiers.org/hco/2/GRCh38#157306966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57923492-C-A

157307142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923643-A-G

157307226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, undefined
orthologous variants: 57923725-T-A

157307260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923759-G-C

157307292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923792-G-A

157307304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57923804-A-G

157307551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924020-C-T

157307562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924027-C-T

157307596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924061-C-T

157307599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924064-A-G

157307786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924422-T-C

157308061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924744-A-T

157308262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57924955-A-T

157308475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925119-T-C

157308494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925138-A-G

157308494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925138-A-T

157308532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925176-G-A

157308532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925176-G-C

157308532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925176-G-T

157308644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: synonymous variant
orthologous variants: 57925288-A-G

157308653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: synonymous variant
orthologous variants: 57925297-G-A

157308653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: missense variant
orthologous variants: 57925297-G-C

157308719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: synonymous variant
orthologous variants: 57925363-T-C

157308805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925434-A-G

157308826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925455-T-C

157308826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925455-T-G

http://identifiers.org/hco/2/GRCh38#157308855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57925488-A-C

157308855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925488-A-T

157309056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925703-G-A

157309078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925725-A-G

http://identifiers.org/hco/2/GRCh38#157309088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57925735-C-A

http://identifiers.org/hco/2/GRCh38#157309131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57925778-A-C

157309201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57925851-G-A

157309444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57926004-T-G

157310352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57927686-A-G

157310356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57927690-G-C

157310376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57927710-G-A

157310402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928016-A-G

157310453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928067-A-G

157310477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928089-A-G

157310488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928100-T-C

157310490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928102-A-G

157310772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928417-A-G

http://identifiers.org/hco/2/GRCh38#157310893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57928560-A-C

157310936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928598-A-G

157311071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928705-T-A

157311071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron variant
orthologous variants: 57928705-T-C

157311161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 57928777-T-C

157311161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, splice_region_variant, stop_gained
orthologous variants: 57928777-T-G

http://identifiers.org/hco/2/GRCh38#157311170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#57928786-C-A

157311170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, missense_variant
orthologous variants: 57928786-C-T

157311178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, missense_variant
orthologous variants: 57928794-G-A

157311178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, missense_variant
orthologous variants: 57928794-G-T

http://identifiers.org/hco/2/GRCh38#157311202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57928818-C-A

157311202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 57928818-C-T

157311372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57928983-G-A

157311372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57928983-G-T

157311487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929099-A-G

157311487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929099-A-T

http://identifiers.org/hco/2/GRCh38#157311499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57929111-C-A

http://identifiers.org/hco/2/GRCh38#157311524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57929136-C-A

http://identifiers.org/hco/2/GRCh38#157311554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57929163-C-A

http://identifiers.org/hco/2/GRCh38#157311582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57929192-C-A

157311582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929192-C-T

http://identifiers.org/hco/2/GRCh38#157311583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57929193-A-C

157311583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929193-A-G

157311622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929232-A-G

157311792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929349-G-A

157311869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929417-A-G

157311936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929481-A-G

157311973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929520-A-T

157312210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929801-G-T

http://identifiers.org/hco/2/GRCh38#157312231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57929822-C-A

157312326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929925-G-C

157312326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929925-G-T

157312328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929927-G-A

157312357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929949-G-T

157312390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57929973-A-G

http://identifiers.org/hco/2/GRCh38#157312425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930009-A-C

157312425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930009-A-T

157312440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930024-G-A

157312449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930033-A-G

http://identifiers.org/hco/2/GRCh38#157312506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930095-C-A

http://identifiers.org/hco/2/GRCh38#157312517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930106-C-A

157312643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930226-T-C

157312753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930330-A-T

157312765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930341-A-G

http://identifiers.org/hco/2/GRCh38#157312776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930354-C-A

157312865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930437-T-A

http://identifiers.org/hco/2/GRCh38#157312923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930468-C-A

157312937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930481-T-C

157313000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930539-A-G

http://identifiers.org/hco/2/GRCh38#157313472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930667-C-A

157313472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930667-C-T

157313497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930685-G-A

157313497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930685-G-T

157313504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930692-G-A

157313504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930692-G-T

http://identifiers.org/hco/2/GRCh38#157313578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57930768-C-A

157313578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930768-C-G

157313631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930822-C-T

157313710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930897-A-G

157313737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930943-T-C

157313792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57930996-C-T

157313976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931173-C-G

157314048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931756-G-A

157314048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931756-G-C

157314062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931770-G-T

157314184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931877-G-A

157314184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931877-G-T

157314290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57931985-C-T

157314317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57932012-T-A

157314317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57932012-T-C

157314548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57932248-T-C

http://identifiers.org/hco/2/GRCh38#157314732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57932433-A-C

157314732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57932433-A-T

157316662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57933369-G-C

157316826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57933518-A-G

157316965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57933648-A-G

157317286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57933899-T-C

http://identifiers.org/hco/2/GRCh38#157317591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#57934154-A-C

157317740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4127
most severe consequence: 3 prime UTR variant
orthologous variants: 57934309-C-T