151428817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219037-A-G

http://identifiers.org/hco/3/GRCh38#151428942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59219158-C-A

151429119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219344-G-C

151429134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219363-G-A

151429382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219592-C-G

151429461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219666-T-A

151429508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219702-G-A

151429561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219748-C-G

151429591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219778-C-T

151429851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219963-A-G

151429864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59219976-G-T

151431193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59221227-C-T

151431261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59221293-G-T

151432679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59222050-G-A

151432679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59222050-G-C

151432679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59222050-G-T

151432744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 59222110-C-G

151432744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 59222110-C-T

151432807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 59222173-C-T

151432818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222181-G-C

151432889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222245-G-A

151432889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222245-G-T

http://identifiers.org/hco/3/GRCh38#151432944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59222302-A-C

151432944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222302-A-T

http://identifiers.org/hco/3/GRCh38#151433153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59222481-A-C

151433153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222481-A-T

151433232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222530-G-C

http://identifiers.org/hco/3/GRCh38#151433243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59222541-C-A

151433243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222541-C-G

151433243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222541-C-T

151433252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222549-A-G

151433253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222550-C-G

151433253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222550-C-T

151433390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59222694-G-T

151433848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59223152-G-A

http://identifiers.org/hco/3/GRCh38#151434384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59223685-C-A

151434384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59223685-C-T

151434607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59223892-G-T

151434952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59224260-T-C

151434973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59224288-G-C

151435328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59224590-G-T

151435755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225000-A-T

151435896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225082-A-G

151435966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225149-T-G

151436099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225282-C-T

151436425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225622-T-C

151436440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225638-T-C

151436440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59225638-T-G

http://identifiers.org/hco/3/GRCh38#151436533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59225726-A-C

151436669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225867-G-A

151436669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225867-G-T

151436672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225870-G-A

151436672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225870-G-T

http://identifiers.org/hco/3/GRCh38#151436701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59225899-A-C

151436701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59225899-A-T

151436724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225922-T-C

151436728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59225926-A-G

http://identifiers.org/hco/3/GRCh38#151436737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59225935-C-A

151436737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225935-C-G

151436771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225969-G-C

151436772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225970-T-C

151436772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59225970-T-G

151436788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59225986-G-T

151437127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226325-T-C

151437139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226337-T-A

151437139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226337-T-C

151437148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226346-A-T

http://identifiers.org/hco/3/GRCh38#151437157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59226355-C-A

151437157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59226355-C-T

151437214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226412-A-T

151437385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59226583-G-C

151437502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59226700-C-G

151437658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59226856-C-G

151437667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226865-C-T

151437688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226886-T-A

151437688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226886-T-C

151437715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226913-T-C

151437715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59226913-T-G

151437969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59227167-A-G

151438231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59227429-C-T

151438384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59227582-A-G

http://identifiers.org/hco/3/GRCh38#151438405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59227603-A-C

151438405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59227603-A-G

151439302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59228779-T-G

http://identifiers.org/hco/3/GRCh38#151441367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59232370-A-C

151441396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232399-A-T

151441511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232508-G-A

151441659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232658-C-T

151442929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232801-G-C

151442929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232801-G-T

http://identifiers.org/hco/3/GRCh38#151442938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59232816-C-A

151442938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232816-C-G

151442938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59232816-C-T

151442998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59232870-G-T

151443032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: 59232904-T-C

151443032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: 59232904-T-G

151443391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59233263-A-G

151443424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59233296-T-G

151443444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: 59233316-T-A

151443505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59233377-G-A

151443505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: 59233377-G-T

151443519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: 59233391-G-A

151443574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59233446-G-A

151443574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59233446-G-C

151443670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59233542-G-A

151443748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59233620-G-T

151443793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59233665-G-A

151443905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59233777-T-C

http://identifiers.org/hco/3/GRCh38#151443962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59233804-C-A

151443978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59233820-T-A

151444681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: -T-C

151444697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: -T-C

151444827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59235122-A-T

http://identifiers.org/hco/3/GRCh38#151444858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59235151-C-A

151444868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59235160-T-A

151444884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59235176-A-G

151445089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235375-G-C

151445191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235474-G-A

151445238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59235521-T-C

151445276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235559-G-A

151445291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235574-T-C

151445318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235601-G-C

151445448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous_variant, undefined
orthologous variants: 59235713-G-A

151445448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense_variant, undefined
orthologous variants: 59235713-G-C

151445482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235747-T-C

151445601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59235866-T-C

151445601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59235866-T-G

151445637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59235890-C-G

151445786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236033-C-T

151445789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236036-G-C

151445868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59236085-G-A

151446094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236302-G-A

151446094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236302-G-C

151446202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236410-A-G

151446315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236523-T-A

151446331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236539-C-G

151446331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236539-C-T

151446378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59236586-C-T

151446457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: stop gained
orthologous variants: 59236668-G-C

151446493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236704-G-A

151446542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236753-G-A

151446542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236753-G-C

151446542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236753-G-T

http://identifiers.org/hco/3/GRCh38#151446561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59236772-A-C

151446592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236803-C-G

151446620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236831-T-C

151446629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236846-T-C

151446651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59236868-T-C

151446651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59236868-T-G

http://identifiers.org/hco/3/GRCh38#151446721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59236938-A-C

151446754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236971-G-T

151446769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59236986-C-G

151446810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237027-T-A

151446810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237027-T-C

151446866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59237083-A-T

151446971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59237170-T-C

http://identifiers.org/hco/3/GRCh38#151447071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#59237273-A-C

151447112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59237314-A-G

http://identifiers.org/hco/3/GRCh38#151447210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59237424-A-C

151447218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237432-T-C

151447218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237432-T-G

http://identifiers.org/hco/3/GRCh38#151447239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59237453-C-A

151447239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237453-C-T

151447345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: stop gained
orthologous variants: 59237544-G-C

151447390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59237589-G-A

151447390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59237589-G-C

151447416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237615-T-C

151447554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237753-C-G

151447554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237753-C-T

151447563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237762-A-G

151447596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59237795-A-G

151447802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: stop gained
orthologous variants: 59238001-G-A

151447839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238038-G-A

151447839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238038-G-C

151447885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238084-C-T

151447901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238100-G-A

151447901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238100-G-C

151447901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238100-G-T

151447978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238177-C-T

151447995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238194-G-C

151447995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238194-G-T

151448049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238248-G-A

151448073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238272-G-A

151448073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238272-G-T

151448123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238322-T-C

http://identifiers.org/hco/3/GRCh38#151448150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#59238349-C-A

151448150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238349-C-T

151448193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238392-A-G

151448212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238411-G-A

151448212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238411-G-C

151448339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238538-C-T

151448488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238687-G-A

151448510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238709-C-T

151448535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59238734-C-G

151448535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238734-C-T

151448553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238752-T-G

151448619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238818-A-G

151448655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238854-G-A

151448655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238854-G-C

151448703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238902-G-A

151448790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59238989-T-C

151448815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59239014-T-C

151448847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59239046-C-G

151448859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59239058-C-T

151448914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59239113-G-A

151448927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59239126-T-C

151449113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59239312-A-G

http://identifiers.org/hco/3/GRCh38#151449302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59239506-C-A

151449302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239506-C-T

151449338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239543-G-A

151449338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239543-G-C

151449338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239543-G-T

151449591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239798-T-C

151449640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239835-T-C

151450026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239994-A-G

151450042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59239998-G-A

151450165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59240064-A-T

151450284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59240196-G-A

151450425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59240318-C-G

151450573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241060-G-A

151450951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241126-G-A

http://identifiers.org/hco/3/GRCh38#151451135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59241318-A-C

151451138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241321-C-T

151451211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241397-A-T

151451506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241665-G-C

151451712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241739-T-G

151451774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59241788-T-C

151452093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242048-G-A

151452093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242048-G-C

151452202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242156-C-G

151452204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242158-T-C

http://identifiers.org/hco/3/GRCh38#151452257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59242180-C-A

151452495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242368-T-C

151452574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242426-T-G

151452641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242452-G-A

151452845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242567-T-C

151452910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242636-G-A

151452910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242636-G-T

http://identifiers.org/hco/3/GRCh38#151453271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59242942-C-A

151453271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242942-C-G

151453321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59242990-T-C

151453380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59243614-A-G

151453541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59243775-G-C

151453541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59243775-G-T

151453649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59243883-A-G

http://identifiers.org/hco/3/GRCh38#151453763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59243997-C-A

151453763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59243997-C-G

151453763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense variant
orthologous variants: 59243997-C-T

http://identifiers.org/hco/3/GRCh38#151453774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59244008-C-A

151453774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 59244008-C-T

151453787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59244020-A-G

151453821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59244054-C-T

151453830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59244064-G-A

151453877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59244108-A-G

151453917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59244140-A-G

http://identifiers.org/hco/3/GRCh38#151455778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59245457-C-A

151455852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59245560-T-A

151455919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59245633-G-T

151455987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59245697-A-T

151455995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59245705-G-A

151456045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59245754-A-G

151456175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59245879-A-G

151456331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59246018-A-G

151456461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59246139-C-T

151456503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59246178-T-C

151456575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59246250-A-T

http://identifiers.org/hco/3/GRCh38#151456894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59246969-C-A

151456894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59246969-C-G

151456894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59246969-C-T

151456931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247006-T-C

151456944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247020-T-C

151456971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247045-T-C

151457044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: synonymous variant
orthologous variants: 59247115-T-G

151457179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247247-G-A

151457180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247248-G-A

151457194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247261-T-C

151457195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247262-G-T

http://identifiers.org/hco/3/GRCh38#151457220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59247287-C-A

151457737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59247912-G-A

151457832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248006-T-A

151457876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248023-C-T

151458276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248356-T-A

151458276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248356-T-G

http://identifiers.org/hco/3/GRCh38#151458483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59248527-C-A

151458483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248527-C-G

151458494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248538-G-A

151458725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248769-T-C

151458734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248776-G-A

151458734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248776-G-C

151458734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248776-G-T

151458795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248841-A-G

151458834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59248881-T-C

151458922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59250164-C-T

151459700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59250785-T-A

151459896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59250820-G-C

http://identifiers.org/hco/3/GRCh38#151459961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59250845-A-C

151459993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59250876-C-T

151460001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59250883-C-T

151460349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_acceptor_variant
orthologous variants: 59251189-T-C

http://identifiers.org/hco/3/GRCh38#151460444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59251285-C-A

151460444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron_variant, missense_variant
orthologous variants: 59251285-C-T

151461088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59251849-G-A

151461088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59251849-G-C

151461088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59251849-G-T

151461151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59251902-C-T

151461160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59251911-C-T

151461184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59251912-A-G

151461283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59252001-G-A

151461321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59252039-T-C

http://identifiers.org/hco/3/GRCh38#151461552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59252929-C-A

151461552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59252929-C-T

151461579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59252952-C-T

151461589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59252962-G-T

151461822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59253184-C-T

151461865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59253224-A-G

http://identifiers.org/hco/3/GRCh38#151461910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59253249-C-A

151462269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59253459-G-A

http://identifiers.org/hco/3/GRCh38#151462324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#59253482-C-A

151462344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59253503-A-G

151462581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59253804-T-C

151462770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59253987-G-T

151463516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59254607-T-G

151463524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26384
most severe consequence: intron variant
orthologous variants: 59254615-T-G