14147917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84668407-G-A

14147917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84668407-G-T

14147930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84668394-G-A

14147930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84668394-G-T

14147958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84668366-A-G

14148298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84668059-T-C

14148390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84667951-G-A

http://identifiers.org/hco/19/GRCh38#14148469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84667861-C-A

14148579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84667785-G-A

http://identifiers.org/hco/19/GRCh38#14148652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84667715-C-A

14148682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84667685-T-C

14148847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84667524-G-A

14148847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84667524-G-T

14149038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84667338-G-T

14150150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84666413-T-C

14150333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84666218-T-C

14150333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84666218-T-G

http://identifiers.org/hco/19/GRCh38#14150374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84666165-A-C

http://identifiers.org/hco/19/GRCh38#14150596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84665969-C-A

14150596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84665969-C-G

14150669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84665903-G-A

14150669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84665903-G-T

14150854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84665731-C-G

14150854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84665731-C-T

14150973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84665613-T-C

http://identifiers.org/hco/19/GRCh38#14151321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84665265-C-A

http://identifiers.org/hco/19/GRCh38#14151419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84665173-C-A

http://identifiers.org/hco/19/GRCh38#14151504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84665088-C-A

14151504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84665088-C-G

14151650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664950-G-A

14151650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664950-G-C

14151668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664933-G-A

14151668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664933-G-C

14151668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664933-G-T

14151931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664720-C-T

14151944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664716-C-G

14152072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664621-A-G

14152242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664493-A-G

14152250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664485-G-A

14152317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84664396-T-C

14152374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84664339-T-A

14152440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84664273-G-A

14152463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84664246-G-A

14152546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84664155-T-C

14154880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84663246-G-A

14155079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84663023-T-C

14155097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84663006-A-G

http://identifiers.org/hco/19/GRCh38#14155154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84662969-C-A

14155154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 84662969-C-T

14155159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84662964-T-C

14155230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84662912-G-A

14155230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84662912-G-C

14155230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84662912-G-T

http://identifiers.org/hco/19/GRCh38#14155268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84662885-C-A

14155269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84662884-T-C

14155285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84662872-T-C

http://identifiers.org/hco/19/GRCh38#14155326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84662833-A-C

http://identifiers.org/hco/19/GRCh38#14155633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84662576-C-A

14155633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84662576-C-T

14155635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84662574-G-T

14155747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84662540-T-C

14155837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662456-G-A

14155856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662437-A-G

14155870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662429-G-T

http://identifiers.org/hco/19/GRCh38#14155903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84662411-C-A

14155903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662411-C-T

14155909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662405-G-A

14155909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662405-G-T

14155924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662394-A-G

http://identifiers.org/hco/19/GRCh38#14155931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84662387-C-A

14155931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662387-C-G

14156229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84662140-G-T

14156626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661781-T-C

14156890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661601-G-T

14156896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661592-G-A

14156913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661575-G-A

14156913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661575-G-T

14156914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661574-T-C

14156946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84661544-C-T

14157160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661330-G-A

14157179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661315-C-G

14157179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661315-C-T

14157184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661310-C-T

14157205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661297-C-G

14157205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84661297-C-T

14157329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84661185-G-A

14157329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84661185-G-T

http://identifiers.org/hco/19/GRCh38#14157585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84660953-C-A

14157585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660953-C-G

14157585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660953-C-T

http://identifiers.org/hco/19/GRCh38#14157609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84660926-C-A

14157609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84660926-C-G

14157609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84660926-C-T

14157730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660836-A-G

http://identifiers.org/hco/19/GRCh38#14157731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84660835-C-A

14157731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660835-C-G

14157731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660835-C-T

14157750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660816-G-T

14157762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660804-G-A

14158165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660404-G-T

http://identifiers.org/hco/19/GRCh38#14158240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84660363-C-A

14158240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84660363-C-G

14158330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84660275-C-T

14159390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84659329-G-A

14159391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84659328-T-C

14159502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84659217-T-C

http://identifiers.org/hco/19/GRCh38#14159922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84658895-C-A

14159922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84658895-C-T

14159935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84658882-C-T

14160039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84658805-G-A

14160039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84658805-G-T

14160350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658547-C-T

14160438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658492-G-A

14160438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658492-G-T

14160514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658414-G-A

14160514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658414-G-T

14160547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658381-T-C

14160547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84658381-T-G

14160774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84658188-A-G

http://identifiers.org/hco/19/GRCh38#14161060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84658006-C-A

http://identifiers.org/hco/19/GRCh38#14161219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84657914-C-A

14161219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657914-C-T

http://identifiers.org/hco/19/GRCh38#14161439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84657776-C-A

14161439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84657776-C-G

14161439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84657776-C-T

14161542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84657673-G-A

14161542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84657673-G-T

14161642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657568-G-A

14161642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657568-G-C

14161642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657568-G-T

14161644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657566-G-T

14161688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657525-G-A

14161688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657525-G-T

http://identifiers.org/hco/19/GRCh38#14161755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84657456-A-C

14161755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657456-A-G

14161777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657449-C-G

14161777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657449-C-T

14161961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657332-C-T

14162320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657132-G-A

14162368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84657077-G-A

14162592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84656902-T-G

14162647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 84656850-A-G

14163262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84656235-T-C

14163423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84656074-G-A

14163423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84656074-G-T

http://identifiers.org/hco/19/GRCh38#14163539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84655985-C-A

14163539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84655985-C-T

14163758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84655777-G-A

14164455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84655174-G-A

http://identifiers.org/hco/19/GRCh38#14164831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84654806-C-A

14164831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84654806-C-T

14165035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84654643-G-A

14166356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84653604-G-A

14167329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84652607-T-C

14167534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84652433-G-C

14167534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84652433-G-T

14167579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84652391-C-T

14167595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84652375-C-G

14167883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84652082-G-A

14168798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84651268-G-A

http://identifiers.org/hco/19/GRCh38#14168849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84651236-C-A

14168944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84651143-A-G

14169024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84651068-T-C

14169491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650642-G-C

14169547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650585-A-G

http://identifiers.org/hco/19/GRCh38#14169741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84650392-C-A

14169741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650392-C-T

14169841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650294-G-A

14169841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650294-G-T

14169877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650272-G-T

14169930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650224-G-A

14169930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650224-G-T

14170047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650146-A-G

http://identifiers.org/hco/19/GRCh38#14170049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84650144-C-A

14170308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650076-G-A

14170308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650076-G-C

14170308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650076-G-T

14170398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84650015-A-T

14170580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84649845-G-T

14170616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84649799-G-T

http://identifiers.org/hco/19/GRCh38#14170904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84649536-A-C

14171514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84649429-T-C

14177531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 84645660-C-G

14177560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84645631-C-T

14177777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84645419-G-T

http://identifiers.org/hco/19/GRCh38#14177862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84645362-C-A

14177862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84645362-C-T

14182604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84642950-C-T

14183103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84642544-G-A

14183324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84642355-G-C

14183324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84642355-G-T

14183550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: missense variant
orthologous variants: 84642178-A-G

14183550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: missense variant
orthologous variants: 84642178-A-T

14183707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84642024-G-A

14183707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84642024-G-T

14183760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84641963-G-A

14183760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84641963-G-T

http://identifiers.org/hco/19/GRCh38#14195230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84636297-A-C

14195233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84636294-C-T

14195291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84636232-C-T

http://identifiers.org/hco/19/GRCh38#14195427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#84636117-C-A

14195427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84636117-C-T

14195545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84636019-G-A

14195545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84636019-G-C

14195608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84635957-C-T

14195620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84635952-C-T

14202585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84630736-G-C

14202758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84630561-G-A

14203178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84630214-T-C

14205199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84628207-G-C

14205459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84627952-A-G

14205482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84627910-G-A

14205967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84627569-G-A

14205967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: intron variant
orthologous variants: 84627569-G-T

14206170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20973
most severe consequence: 5 prime UTR variant
orthologous variants: 84627363-G-A