36281641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969026-G-A

36281641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969026-G-T

36281656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969041-A-G

36281681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969068-T-C

36281681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969068-T-G

36281704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969091-G-A

36281753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62969143-C-T

36281806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62969197-G-A

36281835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969226-A-G

36281836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969227-G-T

36281856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969247-A-G

36281864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969255-G-A

36281864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 62969255-G-T

36281870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969261-G-A

36281870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969261-G-C

36281870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969261-G-T

36281905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62969296-T-C

36281929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62969320-C-T

36282016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62969407-T-C

36282016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62969407-T-G

36282054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969452-T-C

36282074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969471-G-A

36282074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969471-G-T

36282111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969508-A-T

36282126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969522-G-T

36282170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969566-G-T

36282297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969679-G-C

36282297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969679-G-T

36282641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970018-G-T

36282701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62970069-T-G

36282799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970155-T-C

36282832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970188-C-T

http://identifiers.org/hco/4/GRCh38#36283333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62970599-C-A

36283673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970892-C-T

36283688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970905-A-G

36283782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971004-T-C

36283783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971005-G-A

36283783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971005-G-T

36283791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971015-T-A

36283791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971015-T-C

http://identifiers.org/hco/4/GRCh38#36284010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62971154-A-C

36284025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62971169-G-A

36284154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62971298-A-T

http://identifiers.org/hco/4/GRCh38#36284195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62971339-C-A

36284195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62971339-C-G

36284217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62971361-C-T

36284288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62971432-C-T

36284383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62971527-A-G

36284578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62971719-A-G

36284578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62971719-A-T

36284606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971747-T-C

36284606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971747-T-G

36284618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971761-T-C

http://identifiers.org/hco/4/GRCh38#36284627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62971770-C-A

36284627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971770-C-T

36284640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971783-G-C

36285126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972075-G-A

36285126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972075-G-T

36285233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972177-T-G

36285414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972356-A-G

36285548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972512-C-T

http://identifiers.org/hco/4/GRCh38#36285676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62972638-C-A

36285709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972671-A-G

36285830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972810-C-T

36286054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973035-G-A

36286217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62973187-C-G

36286299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62973268-C-T

36286489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973456-T-G

http://identifiers.org/hco/4/GRCh38#36286499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62973466-C-A

36289103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973908-A-G

http://identifiers.org/hco/4/GRCh38#36289107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62973912-C-A

36289107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973912-C-T

36289135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973937-G-A

36289185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973986-C-G

36289312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974116-G-C

36289427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974230-T-G

36289574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974381-C-T

36289603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974418-T-C

36289646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974460-T-C

http://identifiers.org/hco/4/GRCh38#36289908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62974694-C-A

http://identifiers.org/hco/4/GRCh38#36289950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62974730-C-A

http://identifiers.org/hco/4/GRCh38#36290014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62975465-A-C

36290117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975613-C-G

36290117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975613-C-T

36290227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975715-G-T

36290229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975717-G-A

36290229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975717-G-T

36290293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975783-G-C

36290293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975783-G-T

http://identifiers.org/hco/4/GRCh38#36290302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62975792-C-A

36290302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975792-C-G

36290302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975792-C-T

36290327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975817-C-T

36290343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62975833-G-T

http://identifiers.org/hco/4/GRCh38#36290432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62975941-C-A

http://identifiers.org/hco/4/GRCh38#36290534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62976043-A-C

36290640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62976149-C-T

http://identifiers.org/hco/4/GRCh38#36290735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62976244-C-A

36290936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976594-T-C

http://identifiers.org/hco/4/GRCh38#36292292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62977975-A-C

36292788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978438-A-G

http://identifiers.org/hco/4/GRCh38#36293035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62978683-C-A

36293035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978683-C-T

36293192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978837-G-A

36293431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979110-G-A

36293431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979110-G-C

http://identifiers.org/hco/4/GRCh38#36293450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62979143-A-C

36293474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979167-T-C

36293612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62979313-G-T

http://identifiers.org/hco/4/GRCh38#36293782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62979450-A-C

36293805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979473-A-G

36294366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62983940-C-T

http://identifiers.org/hco/4/GRCh38#36294409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62983972-C-A

36294453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984026-A-G

36294489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984064-A-G

36294674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984220-A-G

36294677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984223-A-G

36294677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984223-A-T

http://identifiers.org/hco/4/GRCh38#36294697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62984239-C-A

36294745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984275-G-A

36294745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984275-G-C

36294745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984275-G-T

http://identifiers.org/hco/4/GRCh38#36294750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62984280-C-A

36294750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984280-C-T

36294756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984286-T-C

36294782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984349-A-G

36294890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62984457-G-A

36294917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62984484-G-A

36294932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62984499-T-A

36295046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62984621-A-T

36295072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984647-A-G

http://identifiers.org/hco/4/GRCh38#36295108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62984680-C-A

36295108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984680-C-T

http://identifiers.org/hco/4/GRCh38#36295133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62984706-C-A

36295135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984708-G-T

http://identifiers.org/hco/4/GRCh38#36295188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62984747-A-C

36295188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62984747-A-G

36300067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62985858-T-A

36300266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986072-G-C

36300282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986088-A-G

36300630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986411-C-G

36300630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986411-C-T

36300658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986455-T-A

36300658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986455-T-C

36300665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986462-G-T

36300684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986481-T-C

36300684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986481-T-G

36300689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986486-T-C

36300695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986495-A-T

36300696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986496-G-C

36300765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986566-C-T

36301072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986851-T-C

36301182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987056-G-A

36301206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987079-C-T

36301397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987301-C-T

36301409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987313-T-G

36301658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987531-A-G

36301780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987652-G-C

36301873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987799-G-A

36301944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987880-C-T

36302218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62988117-G-A

36302498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62988499-G-A

36302498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62988499-G-T

36302778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989059-T-C

36302921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989192-C-T

36303072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989325-G-T

36303112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989356-C-T

36303354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994208-T-C

http://identifiers.org/hco/4/GRCh38#36303477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62994337-C-A

http://identifiers.org/hco/4/GRCh38#36303530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62994382-C-A

36303642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994495-T-C

36303704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994545-C-T

36303772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994614-C-T

http://identifiers.org/hco/4/GRCh38#36303822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62994659-C-A

36303939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994773-A-T

36304006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994825-G-A

36304143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994967-C-T

36304167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994978-A-G

http://identifiers.org/hco/4/GRCh38#36304250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62995074-C-A

36305670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996043-T-C

http://identifiers.org/hco/4/GRCh38#36305770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62996129-A-C

http://identifiers.org/hco/4/GRCh38#36305908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62996251-C-A

36306005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996356-C-T

36306022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996417-A-T

36306035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996431-T-C

36306161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996558-A-G

36306185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62996577-A-T

36306201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62996593-G-T

36306226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62996618-A-G

36306265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62996657-A-G

36306299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62996694-G-T

http://identifiers.org/hco/4/GRCh38#36306419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#62996812-A-C

36306761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62997164-A-G

36306856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62997258-G-A

36306907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62997308-G-A

36308058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63000039-T-A

36308217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63000174-C-T

36308240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63000197-T-C

36308315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63000272-C-T

36308327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63000284-T-C

36308392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63000349-A-G

36308534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63000488-A-G

36308571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63000524-G-T

http://identifiers.org/hco/4/GRCh38#36310372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63001885-C-A

36310372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001885-C-T

36310569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002073-T-C

36310572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002076-T-G

36310695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002178-G-A

36310913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63002326-G-A

36311029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002434-G-A

36311063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002467-T-C

36311075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002479-A-G

36311091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002495-G-T

36311141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002532-G-A

36311194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63002585-G-T

http://identifiers.org/hco/4/GRCh38#36311213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63002604-C-A

36311213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63002604-C-T

36311382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002714-T-C

36311461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002781-T-C

36311461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002781-T-G

http://identifiers.org/hco/4/GRCh38#36311466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63002788-A-C

36311526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002831-T-C

36311561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002884-G-A

36311561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002884-G-T

36311774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63003051-C-T

36311817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003088-T-A

36311854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003118-G-T

36311884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003151-T-C

36311929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003210-G-T

http://identifiers.org/hco/4/GRCh38#36311968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63003249-C-A

36312002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003285-T-C

36312037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003320-G-A

36312064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003346-G-C

36312121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003404-T-A

36312143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003430-G-A

36312225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003518-A-G

36312410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003689-A-G

36312439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003714-G-A

36312560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63003817-G-C

36312878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004052-T-G

36312928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004102-T-A

36313141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004325-A-G

36313149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004333-T-C

36313402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004573-A-G

36313411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004582-A-G

36313411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004582-A-T

36313438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004596-T-A

36313438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004596-T-C

36313485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004641-G-T

36313517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004669-T-C

36313545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004697-C-G

36313546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004698-T-C

36313559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004711-A-G

36313580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004733-A-T

http://identifiers.org/hco/4/GRCh38#36313583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63004736-A-C

36313649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004792-T-A

http://identifiers.org/hco/4/GRCh38#36313664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63004804-C-A

36314127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005241-T-C

36314135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005249-G-T

36314215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005326-T-C

36314809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005548-A-T

36314936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005675-G-C

36314936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005675-G-T

36315009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005735-A-G

36315170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005878-T-C

36315289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005965-T-C

36315309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005985-G-T

36315388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006059-T-A

36315545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006626-T-A

36315545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006626-T-G

http://identifiers.org/hco/4/GRCh38#36315548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63006629-C-A

36315614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006710-G-A

36315614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006710-G-T

36315625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006721-G-C

36315672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006767-G-T

http://identifiers.org/hco/4/GRCh38#36315682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63006777-A-C

36315682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006777-A-T

36315710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006804-T-C

36315742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63006836-A-G

36315818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006921-C-G

36315830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006936-G-A

36315830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006936-G-C

36316495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007316-T-C

36316580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007395-T-A

36316585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007400-G-T

36316595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007410-G-T

36316620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007435-G-A

36316734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007549-T-C

36316939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007755-G-T

36317111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007915-C-T

36317115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007919-C-G

36317136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007939-C-T

36317276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008185-G-T

36317330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008238-C-T

http://identifiers.org/hco/4/GRCh38#36317441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63008307-C-A

36317702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008495-A-G

http://identifiers.org/hco/4/GRCh38#36317708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63008501-A-C

36318054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008814-C-T

36318085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008844-A-G

http://identifiers.org/hco/4/GRCh38#36318123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63008885-C-A

36318123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008885-C-T

36318239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009000-G-T

36318327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009088-T-C

36318577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009336-A-G

36318591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009350-T-C

36318599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009358-T-C

36319062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010214-A-G

36319340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010403-G-A

36319616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010655-G-A

36319642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010680-G-A

36319653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010691-G-A

36319653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010691-G-C

http://identifiers.org/hco/4/GRCh38#36319877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63010905-C-A

36319905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010928-C-T

36319937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63010960-G-A

36320007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011030-G-A

36320137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011182-C-T

36320508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011940-T-C

36320582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012014-C-T

36320771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012213-G-A

36320773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012215-A-T

36321852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014674-C-G

36321995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014818-T-C

36322332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015155-C-G

36322898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015690-G-A

36322976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015767-G-C

36323226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016037-A-G

36323635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016627-G-A

http://identifiers.org/hco/4/GRCh38#36323703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63016767-A-C

36323735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016799-T-C

36323761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016825-T-C

36323778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016842-T-G

36328242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63024425-T-C

36328399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63024588-G-A

36328407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63024596-C-T

36328618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63024749-C-G

http://identifiers.org/hco/4/GRCh38#36328743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63024873-A-C

36328743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63024873-A-G

36329100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63025590-G-A

36329194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63025690-G-A

36329194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63025690-G-C

36329210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63025704-A-G

36329286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63025763-T-G

36329354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032811-A-G

36329457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032906-A-G

36329735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033189-C-T

36329829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033263-A-G

36330104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033500-A-T

http://identifiers.org/hco/4/GRCh38#36330241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63033655-A-C

36330430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033953-A-G

http://identifiers.org/hco/4/GRCh38#36330541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63034042-A-C

36330671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034182-T-C

http://identifiers.org/hco/4/GRCh38#36330715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63034226-C-A

36330810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034283-A-G

36330919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034400-T-C

36331471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034992-C-T

36332267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035251-G-A

36332293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035267-G-T

36332353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035324-A-T

36332518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035502-A-G

36332518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035502-A-T

36332695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035673-T-A

36332695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035673-T-C

36335674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036293-C-T

36335712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036326-G-T

36335730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036344-C-G

36335849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036466-G-A

36335953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036612-C-T

36335988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036649-A-G

36336101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036757-C-T

36336263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036907-T-G

36336270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036914-T-C

36336301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036945-A-G

36336342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036984-C-T

36337633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038077-G-A

36337654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038097-G-T

36338221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038662-A-T

36338287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038727-A-G

36338287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038727-A-T

36338368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038827-T-C

36338412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038869-T-C

36338671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039117-A-G

http://identifiers.org/hco/4/GRCh38#36338908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63039414-C-A

36338988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039492-T-G

36338996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039500-G-T

http://identifiers.org/hco/4/GRCh38#36339037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63039537-A-C

36339037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039537-A-G

36339041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039541-G-T

http://identifiers.org/hco/4/GRCh38#36339063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63039559-A-C

http://identifiers.org/hco/4/GRCh38#36339102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63039597-C-A

36339102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039597-C-T

36339127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63039622-A-G

36339135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 63039630-A-G

36339226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039720-T-C

36339380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039855-G-C

36339461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039932-A-T

36339532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040014-G-A

36339532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040014-G-C

36339695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040246-A-G

36339699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040250-T-G

36340380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041324-A-G

36340418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041925-G-T

36340454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041952-G-A

36340621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042115-T-C

36340713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042216-G-A

36340713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042216-G-T

36340825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042319-A-G

36340960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043111-G-A

36341013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043172-C-T

36341204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043308-T-C

36341323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043373-T-C

36341441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043487-G-T

36341547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043591-T-C

36341741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043748-T-C

36341768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043779-T-A

36341768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043779-T-C

36341814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043823-T-C

36341888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043885-G-A

36341941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043926-G-C

36342116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63044338-G-A

36342317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63044523-G-C

36342317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63044523-G-T

36342448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63044650-T-G

36343363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045159-A-G

36343363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045159-A-T

http://identifiers.org/hco/4/GRCh38#36343367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63045163-A-C

36343367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045163-A-G

36343367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045163-A-T

36343368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045164-G-A

36343368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045164-G-C

36343368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045164-G-T

http://identifiers.org/hco/4/GRCh38#36343389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63045183-C-A

36343389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045183-C-T

http://identifiers.org/hco/4/GRCh38#36343408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63045202-C-A

36343408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045202-C-T

36343415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045209-A-G

36343467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63045257-G-A

http://identifiers.org/hco/4/GRCh38#36343479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63045272-A-C

36343602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63045403-T-G

36343776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63045577-T-A

http://identifiers.org/hco/4/GRCh38#36343814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
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/5/GRCm39#63045615-C-A

36343814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63045615-C-T

http://identifiers.org/hco/4/GRCh38#36343963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63045768-C-A

36343963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63045768-C-G

36343963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63045768-C-T

36344023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046417-G-T

36344024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046418-G-A

36344024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046418-G-T

36344040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046432-T-G

36344053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046445-T-A

36344059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046451-G-T

36344122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046527-G-A

36344122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046527-G-T

36344129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046534-G-A

36344147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046552-T-C

36344182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046583-A-G

http://identifiers.org/hco/4/GRCh38#36344844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63046638-C-A

36344847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046641-A-G

36345041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046803-T-C

36345047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046809-T-C

http://identifiers.org/hco/4/GRCh38#36345090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63046851-A-C

36345090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046851-A-G

36345103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046864-T-C

36345130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63046879-G-T

36345675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63047287-G-T

36345853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63047443-T-C

http://identifiers.org/hco/4/GRCh38#36346002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63047904-C-A

36346154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63048027-A-G

36346183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63048066-C-T

http://identifiers.org/hco/4/GRCh38#36346228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63048129-C-A

36346236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63048137-G-C

36346314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63048210-T-A

http://identifiers.org/hco/4/GRCh38#36346564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#63048782-A-C

36346784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63049003-G-A

36346785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63049004-T-C

36346790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63049009-C-T

36346880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63049077-A-G

36347100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63049270-G-A

36347397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63049533-A-T