http://identifiers.org/hco/7/GRCh38#127344319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28212112-C-A

127344571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28212371-A-T

127345034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28212805-T-G

http://identifiers.org/hco/7/GRCh38#127345133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28212900-C-A

127345926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28213696-C-T

127346300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28214143-T-C

127346340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28214181-T-C

127346343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28214184-A-T

127346427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3 prime UTR variant
orthologous variants: 28214265-G-A

127346839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214660-G-T

http://identifiers.org/hco/7/GRCh38#127346840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28214661-A-C

127346840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214661-A-G

127346841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214662-A-G

127346874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214678-T-C

127346924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214720-T-C

127346945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214740-C-T

127346980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214771-G-A

127346980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214771-G-T

http://identifiers.org/hco/7/GRCh38#127347019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28214806-C-A

127347019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214806-C-T

127347020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214807-A-G

127347020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214807-A-T

127347023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214810-G-A

127347023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214810-G-T

127347034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214821-A-G

http://identifiers.org/hco/7/GRCh38#127347061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28214848-C-A

127347061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214848-C-G

127347061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28214848-C-T

127347207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28215003-A-G

127347243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28215039-G-C

http://identifiers.org/hco/7/GRCh38#127347652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#28215324-C-A

127347652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215324-C-G

127347652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215324-C-T

127347676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215343-G-A

127347676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215343-G-T

127347712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215369-A-G

127347715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215372-G-A

127347715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215372-G-T

127347719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215376-A-G

http://identifiers.org/hco/7/GRCh38#127347764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#28215408-C-A

127347764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215408-C-T

127347791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28215433-C-T

127347850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28215479-G-A

127347974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28215599-G-A

127347974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28215599-G-T

127348068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28215668-G-A

127348068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28215668-G-T

127348387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28215920-G-C

127348607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28216096-T-G

127348826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28216301-T-C

127348921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28216374-A-G

http://identifiers.org/hco/7/GRCh38#127349323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28216767-C-A

127349323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28216767-C-T

127349426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28216849-T-C

127349470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28216894-G-A

127349596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28217021-G-A

127349689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28217134-G-A

127349689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28217134-G-T

127349834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28217483-A-G

127349852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28217505-T-C

127349878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28217571-C-G

127349936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28217688-T-C

127349967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28217720-G-T

127350167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28217924-G-T

127350223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28218012-G-A

127350223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28218012-G-T

127350311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28218084-C-T

127350865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28218602-C-G

127350865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28218602-C-T

http://identifiers.org/hco/7/GRCh38#127351332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28219100-C-A

127351332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28219100-C-G

127351336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28219104-G-T

127351415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28219222-T-C

127351610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28219706-T-C

127351640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28219737-G-C

127351940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28220036-A-G

127352017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28220103-A-T

127352065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28220151-T-C

127352108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28220185-A-G

127354700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28223103-T-C

127355222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28223680-A-T

127355527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28223983-T-A

127355646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28224093-A-G

127356195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28224832-C-G

127356447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28225035-A-T

127356480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28225057-T-C

127356652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28225217-C-T

127356729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28225296-G-T

127356781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28225347-G-T

127357174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28225679-T-C

127357612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28226320-T-G

127357878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28226789-G-A

http://identifiers.org/hco/7/GRCh38#127358130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28227020-C-A

127358130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28227020-C-T

http://identifiers.org/hco/7/GRCh38#127358163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28227053-C-A

http://identifiers.org/hco/7/GRCh38#127358181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28227065-C-A

127358352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28227215-C-T

127358488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28227424-C-T

127358820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28227768-A-T

127358832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28227779-A-G

http://identifiers.org/hco/7/GRCh38#127358989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28228096-A-C

127359237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28228330-T-C

127359404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28228457-A-G

127360353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229061-A-G

127360515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229201-T-C

127360677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229455-A-G

127360684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229469-C-T

127360708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229493-T-C

127360715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229538-C-T

127360800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229630-T-C

http://identifiers.org/hco/7/GRCh38#127361023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28229844-C-A

http://identifiers.org/hco/7/GRCh38#127361087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28229907-C-A

127361087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229907-C-T

127361119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229928-C-T

127361146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28229956-G-A

127361582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28230430-T-C

127361589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28230437-G-T

127361667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28230532-T-G

127361762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28230847-A-T

127362260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231282-G-T

127362307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231311-T-A

127362394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231394-G-A

127362394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231394-G-T

127362472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231478-A-G

http://identifiers.org/hco/7/GRCh38#127362475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28231481-C-A

127362547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231511-C-T

127362716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231664-G-A

127362716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28231664-G-T

http://identifiers.org/hco/7/GRCh38#127362814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28231756-C-A

127363087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28232018-G-T

127365281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28232299-G-A

127365670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28232663-T-C

127365974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28232982-C-T

127365977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28232985-T-C

127366101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28233123-C-T

127366295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28233247-A-G

127366384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28233351-T-C

127366691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28233617-T-A

127366966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28233872-A-G

127367207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28234071-G-T

127367246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28234111-C-T

127367339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28234214-G-C

127367339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28234214-G-T

http://identifiers.org/hco/7/GRCh38#127367366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28234240-C-A

127367366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28234240-C-T

127367542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28237526-G-C

http://identifiers.org/hco/7/GRCh38#127367557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28237538-C-A

127367592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28237566-T-G

127367978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28237954-T-C

127368109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238075-T-A

127368109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238075-T-C

127368163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238131-G-C

127368193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238159-G-C

127368392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238322-A-G

127368392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238322-A-T

http://identifiers.org/hco/7/GRCh38#127368745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28238670-C-A

127368834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238748-A-T

127369091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238958-T-C

127369121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28238995-T-A

127369674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28239657-T-A

127369759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28239740-T-C

127369789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28239769-G-C

127369842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28239821-A-G

127370927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28240791-T-C

127371607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28241455-G-C

127371607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28241455-G-T

127372505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242159-T-A

127372505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242159-T-G

127372506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242160-T-G

http://identifiers.org/hco/7/GRCh38#127372542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28242187-C-A

127372542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242187-C-T

127372815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242444-G-T

127373101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242740-C-T

127373278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242915-T-A

127373283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242920-T-A

127373296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28242931-A-T

127373392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28243026-A-G

127373758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: 28243392-A-G

127374030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: missense variant
orthologous variants: 28243664-G-A

127374030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: missense variant
orthologous variants: 28243664-G-T

127374280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: 28243908-A-G

127374306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: stop gained
orthologous variants: 28243931-G-A

127374306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: missense variant
orthologous variants: 28243931-G-C

127374753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: missense variant
orthologous variants: 28244378-G-A

127374790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: 28244418-C-G

127374790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: 28244418-C-T

http://identifiers.org/hco/7/GRCh38#127374811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28244439-A-C

127374811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: 28244439-A-G

127374945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: missense variant
orthologous variants: 28244573-T-C

127374945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: missense variant
orthologous variants: 28244573-T-G

127375037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28244665-G-T

127375341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28244947-G-T

127375396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245002-T-C

127375557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245157-T-C

127375584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245184-A-G

127375712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245281-A-G

127375857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245539-T-C

http://identifiers.org/hco/7/GRCh38#127376035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28245832-A-C

127376035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245832-A-T

127376156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28245949-G-A

127376768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28246717-T-A

127376980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28246959-C-T

127377884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28247790-T-A

127378024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28247921-C-T

http://identifiers.org/hco/7/GRCh38#127378153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28248054-A-C

127378153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28248054-A-G

127379318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28249887-T-C

127379342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28249914-T-A

127379342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28249914-T-C

127379407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28249973-C-T

127379524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28250624-C-T

127379805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28250869-T-C

http://identifiers.org/hco/7/GRCh38#127379853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28250918-C-A

127380056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28251067-C-G

http://identifiers.org/hco/7/GRCh38#127380073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28251082-C-A

127380073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28251082-C-T

127380136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28251125-G-T

127380245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28251232-A-G

127380548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28251416-C-T

127381641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28251929-G-T

http://identifiers.org/hco/7/GRCh38#127381779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28252061-C-A

127381779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28252061-C-T

127383222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, undefined
orthologous variants: 28252989-C-T

127383440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, undefined
orthologous variants: 28253201-T-C

127383513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28253274-G-C

http://identifiers.org/hco/7/GRCh38#127383795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#28253516-C-A

127385339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28255589-G-A

127385339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28255589-G-C

127385383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28255633-T-C

127385575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28256053-T-C

127385621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28256092-G-A

127386115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 28256485-T-C

127386198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28256569-G-A

127386682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28256967-C-T

127386918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28257081-T-C

127386954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28257116-C-T

127387536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28257624-C-G

http://identifiers.org/hco/7/GRCh38#127388000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28257728-A-C

127388157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28257886-A-G

127388191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28257917-G-A

127390706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260003-T-A

127390814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260058-C-T

127391167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260408-T-C

127391237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260476-A-G

http://identifiers.org/hco/7/GRCh38#127391258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28260497-A-C

127391267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260502-T-C

127391429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260643-T-A

127391440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260655-A-G

127391445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260660-G-A

127391445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260660-G-T

http://identifiers.org/hco/7/GRCh38#127391447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28260662-A-C

127391447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260662-A-G

127391448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260663-G-T

127391504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: synonymous variant
orthologous variants: 28260724-A-G

127391659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260881-G-A

127391659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260881-G-C

127391659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28260881-G-T

127391941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261189-G-T

http://identifiers.org/hco/7/GRCh38#127392021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28261251-C-A

127392021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261251-C-T

127392120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261339-G-A

127392120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261339-G-C

127392120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261339-G-T

127392172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261391-G-A

127392172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261391-G-C

127392314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28261546-C-T

http://identifiers.org/hco/7/GRCh38#127392592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28261809-A-C

http://identifiers.org/hco/7/GRCh38#127392655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28261873-C-A

127392893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28262113-G-C

127392921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28262140-G-A

127393059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28262294-C-T

127393087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28262320-G-C

http://identifiers.org/hco/7/GRCh38#127393147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28262359-C-A

127393540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28262727-C-T

127394461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28263879-T-C

127395959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28265150-T-C

127396316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron_variant, undefined
orthologous variants: 28265878-T-G

127396440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28266011-G-C

127399059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285161-C-T

127399164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285237-T-C

127399165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285238-G-A

127399296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285367-C-T

127399305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285376-T-C

127399433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285498-G-A

127399564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28285607-G-C

127399867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28286048-G-A

127400017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28286237-G-A

127400462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28286760-A-G

127400514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28286815-A-G

127400720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28287026-G-C

http://identifiers.org/hco/7/GRCh38#127402949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28290571-C-A

127402949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28290571-C-G

127403151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28290777-T-C

127403210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28290833-G-T

http://identifiers.org/hco/7/GRCh38#127403330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28290968-A-C

127403358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28290991-A-G

127403399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291068-T-C

127403535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291204-T-C

127403635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291300-A-G

127403659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291324-G-C

127403762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291423-G-T

127403984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291625-A-G

127404066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28291703-A-G

http://identifiers.org/hco/7/GRCh38#127404084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28291721-C-A

127404427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292049-G-A

127404493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292156-C-G

127404493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292156-C-T

127404726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292611-G-A

127404782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292666-T-C

127404822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292705-C-T

127405067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292944-G-A

127405111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292979-C-G

127405111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28292979-C-T

127405263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28293040-T-C

127405364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28293125-G-C

http://identifiers.org/hco/7/GRCh38#127406356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28293639-A-C

127406603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28293879-A-G

127406688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28293946-G-A

127406826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28294083-T-C

127406998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28294296-C-T

127407200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28294506-T-C

http://identifiers.org/hco/7/GRCh38#127407272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28295017-A-C

127407388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28295131-C-T

127407487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28295215-C-T

127409423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300212-C-T

127409482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300272-T-A

127409613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300402-T-A

127409685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300483-G-A

127409807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300601-C-T

127409867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300639-T-C

127409898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300670-C-T

127409907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300679-G-A

127409907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300679-G-T

127409985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300743-G-A

127410029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300788-T-A

127410051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300812-T-C

127410074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300835-C-T

127410240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28300988-G-C

127410702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28305322-C-T

127410843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28305457-G-A

http://identifiers.org/hco/7/GRCh38#127410895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28305510-A-C

127410895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28305510-A-G

127410958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28305556-C-T

127411309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306207-T-C

127411450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306341-G-A

127411622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306510-G-A

127411831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306710-G-C

127411844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306723-G-A

127411854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306733-T-C

127411906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306790-T-C

127412028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306910-C-T

127412054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28306932-A-G

127412223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28307095-T-G

127412539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28307391-G-C

127412564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28307416-G-C

127412564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28307416-G-T

127413887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28307950-T-C

127414009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28308067-T-C

http://identifiers.org/hco/7/GRCh38#127414138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28308204-A-C

127414183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28308246-T-C

127414423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309068-C-T

127415130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309160-G-A

127415368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309439-G-A

127415416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309449-T-C

127415457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309492-T-A

127415827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309821-A-G

127415918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309912-T-A

127415918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28309912-T-G

127416216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310191-T-C

127416375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310391-A-G

127416462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310473-G-T

127416574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310585-T-A

127416675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310641-G-T

http://identifiers.org/hco/7/GRCh38#127416693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28310658-A-C

127416700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310664-T-C

127416758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310720-G-C

127416881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28310831-G-A

127418516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28311288-G-A

127418516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28311288-G-C

127418991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28311843-G-C

http://identifiers.org/hco/7/GRCh38#127419284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28312127-C-A

127419385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28312228-A-G

127419509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28312349-G-C

127419639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28312518-G-T

http://identifiers.org/hco/7/GRCh38#127419768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28312658-A-C

127419773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28312663-A-G

127420721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28314506-T-C

127420723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28314508-G-A

127420751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28314536-G-A

127420752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28314537-G-T

127421332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28315894-G-A

127421332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28315894-G-T

127421620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28316184-T-C

127421711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28318545-T-C

127421872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28318798-A-T

http://identifiers.org/hco/7/GRCh38#127430761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28318868-A-C

127430761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28318868-A-T

127430930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319039-G-C

127430943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319052-T-C

127431026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319133-C-T

127431235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319333-T-C

127431536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319639-G-A

127431612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319714-A-T

127431767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319862-T-C

http://identifiers.org/hco/7/GRCh38#127431805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#28319898-C-A

127431821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27267
most severe consequence: intron variant
orthologous variants: 28319914-A-G