77199427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114369842-T-C

77199520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 114369943-G-A

77199520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 114369943-G-C

77199701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370074-C-G

77199701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370074-C-T

http://identifiers.org/hco/16/GRCh38#77199819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114370198-A-C

http://identifiers.org/hco/16/GRCh38#77199976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114370361-C-A

77199976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370361-C-G

77199976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370361-C-T

http://identifiers.org/hco/16/GRCh38#77200001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114370381-C-A

77200001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370381-C-G

http://identifiers.org/hco/16/GRCh38#77200965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114370582-C-A

77200965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370582-C-T

http://identifiers.org/hco/16/GRCh38#77200979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114370596-C-A

77201109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370692-C-T

77201217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370836-G-C

77201268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370881-T-G

77201403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114370999-T-C

77201614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371134-A-G

77201656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371178-T-C

77201673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371197-C-G

77201675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371199-C-G

77201675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371199-C-T

77201681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371205-G-A

77201691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371215-A-T

77201837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371324-A-G

77201972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114371417-A-G

77202102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114371550-A-G

77202406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114371849-C-T

77202490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372136-C-G

77202554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372196-C-T

77202596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372230-T-C

77202598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372232-G-A

77202598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372232-G-T

77202618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372252-G-A

77202819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372332-A-G

77202859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114372370-G-C

77205163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114373981-T-C

http://identifiers.org/hco/16/GRCh38#77205234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114374044-A-C

77205234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374044-A-G

77205241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374051-G-A

77205300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374111-A-G

77205379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374179-C-T

77205476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374264-A-G

77205486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374274-A-T

77205547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114374337-T-C

77206136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114375811-A-T

77206299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114375963-G-A

77206299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114375963-G-T

77206348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376016-G-A

77206348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376016-G-T

http://identifiers.org/hco/16/GRCh38#77206379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114376057-C-A

77206379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376057-C-G

77206387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376065-T-C

http://identifiers.org/hco/16/GRCh38#77206401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114376079-C-A

77206401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376079-C-G

77206401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376079-C-T

http://identifiers.org/hco/16/GRCh38#77206437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114376115-A-C

http://identifiers.org/hco/16/GRCh38#77206444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114376122-A-C

77206444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114376122-A-G

77206597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376269-T-A

77206597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376269-T-G

77206646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376306-G-T

http://identifiers.org/hco/16/GRCh38#77206724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114376553-C-A

http://identifiers.org/hco/16/GRCh38#77206728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114376557-C-A

77206728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376557-C-G

77207244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377149-G-T

77207281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377183-C-T

77207343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377246-G-A

77207389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377295-C-T

77207440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377342-C-T

77207489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377375-A-T

77207659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377525-G-A

77207863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114377898-C-T

77207984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378011-C-T

77208061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378079-T-G

77208124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378144-G-A

77208124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378144-G-T

77208165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378197-A-G

77208235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114378263-G-C

77208382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378343-T-C

77208383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378344-G-A

77208383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378344-G-T

77208432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378348-C-G

77208432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378348-C-T

77208467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114378384-A-G

77208555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378472-A-G

http://identifiers.org/hco/16/GRCh38#77208607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114378534-C-A

77208607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378534-C-G

http://identifiers.org/hco/16/GRCh38#77208608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114378535-A-C

77208611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378538-G-T

77208612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378539-G-A

77208622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378549-G-A

77208622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378549-G-T

http://identifiers.org/hco/16/GRCh38#77208624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114378551-C-A

http://identifiers.org/hco/16/GRCh38#77208628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114378555-C-A

77208629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378556-A-G

http://identifiers.org/hco/16/GRCh38#77208679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114378605-C-A

77208679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378605-C-G

77208679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378605-C-T

77208708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378632-G-C

77208756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378740-C-G

77208842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378885-T-G

77208853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378896-A-G

77208854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378897-G-A

77208921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378973-G-A

77208921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378973-G-C

77208945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114378997-C-G

77208967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379019-G-A

77208967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379019-G-T

http://identifiers.org/hco/16/GRCh38#77208988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379040-C-A

77208988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379040-C-T

77208995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379047-A-G

77208995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379047-A-T

77209000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379052-T-C

77209001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379053-G-A

http://identifiers.org/hco/16/GRCh38#77209009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379054-C-A

77209110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114379158-A-G

77209113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114379161-G-A

77209132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114379180-G-C

http://identifiers.org/hco/16/GRCh38#77209187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379222-C-A

77209190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379225-A-G

77209207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379239-T-A

77209207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379239-T-C

http://identifiers.org/hco/16/GRCh38#77209226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379258-C-A

77209226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379258-C-T

77209233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379265-A-G

http://identifiers.org/hco/16/GRCh38#77209237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379269-C-A

http://identifiers.org/hco/16/GRCh38#77209243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379275-C-A

77209243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379275-C-T

77209281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379323-T-G

http://identifiers.org/hco/16/GRCh38#77209306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379347-C-A

77209306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379347-C-G

http://identifiers.org/hco/16/GRCh38#77209316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379357-C-A

77209316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379357-C-T

http://identifiers.org/hco/16/GRCh38#77209321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379362-C-A

77209321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379362-C-G

77209321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379362-C-T

http://identifiers.org/hco/16/GRCh38#77209485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379523-C-A

77209492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379526-T-A

http://identifiers.org/hco/16/GRCh38#77209547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114379577-A-C

77209557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114379587-A-T

77210980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380456-A-G

http://identifiers.org/hco/16/GRCh38#77210996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114380472-C-A

77210996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380472-C-T

77211081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380530-A-G

77211081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380530-A-T

http://identifiers.org/hco/16/GRCh38#77211104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114380547-C-A

77211104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380547-C-T

77211139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380579-C-T

77211141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380581-T-A

77211141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380581-T-C

77211248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114380708-G-A

77211249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114380709-C-G

77211249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114380709-C-T

77211352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380787-A-T

http://identifiers.org/hco/16/GRCh38#77211403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114380819-C-A

77211403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380819-C-G

77211552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380852-T-C

77211576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380876-G-A

77211576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114380876-G-C

77211607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114380891-G-C

77211631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114380892-C-G

77211714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114380984-A-T

77211743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381014-A-G

77211777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381047-T-C

77211785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381055-G-A

77211840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381104-C-G

77211941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381207-T-G

77211981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381254-A-G

77212021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 114381292-T-A

77212021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 114381292-T-G

http://identifiers.org/hco/16/GRCh38#77212087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381362-A-C

77212106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381374-G-A

77212147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114381414-G-T

77212189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 114381456-G-A

77212189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 114381456-G-C

77212242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114381499-C-T

77212276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 114381534-C-G

77212276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 114381534-C-T

77212339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 114381590-A-G

77212339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 114381590-A-T

http://identifiers.org/hco/16/GRCh38#77212403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381635-C-A

77212403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114381635-C-T

http://identifiers.org/hco/16/GRCh38#77212479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381647-C-A

77212479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381647-C-G

77212479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381647-C-T

http://identifiers.org/hco/16/GRCh38#77212582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381736-C-A

77212582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381736-C-T

77212586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381740-G-T

http://identifiers.org/hco/16/GRCh38#77212598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381752-C-A

77212598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114381752-C-G

77212598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114381752-C-T

http://identifiers.org/hco/16/GRCh38#77212637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381791-C-A

77212637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114381791-C-T

77212652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381806-G-A

77212652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381806-G-C

77212652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381806-G-T

http://identifiers.org/hco/16/GRCh38#77212657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114381810-C-A

77212657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381810-C-G

77212657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381810-C-T

77212695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381858-A-G

77212751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381904-G-A

77212751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381904-G-T

77212782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381945-G-A

77212782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114381945-G-T

77212923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382087-G-A

77212923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382087-G-T

http://identifiers.org/hco/16/GRCh38#77212925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382089-C-A

77212925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114382089-C-T

http://identifiers.org/hco/16/GRCh38#77212928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382093-C-A

77212928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114382093-C-G

77212928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114382093-C-T

77212932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382097-G-A

77212932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382097-G-C

77212932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382097-G-T

http://identifiers.org/hco/16/GRCh38#77212937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382102-C-A

77212937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382102-C-G

77212937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382102-C-T

77213011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382182-G-A

77213011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382182-G-T

77213085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382262-G-A

77213085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382262-G-T

http://identifiers.org/hco/16/GRCh38#77213086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382263-A-C

77213086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382263-A-G

77213086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382263-A-T

http://identifiers.org/hco/16/GRCh38#77213088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382265-C-A

77213088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382265-C-T

http://identifiers.org/hco/16/GRCh38#77213089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382266-C-A

77213089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382266-C-T

http://identifiers.org/hco/16/GRCh38#77213090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382267-C-A

77213090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382267-C-T

77213117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382294-T-A

77213117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382294-T-C

77213117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382294-T-G

http://identifiers.org/hco/16/GRCh38#77213118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114382295-A-C

77213118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382295-A-G

77213118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114382295-A-T