36697901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5 prime UTR variant
orthologous variants: 29333195-G-A

36697901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5 prime UTR variant
orthologous variants: 29333195-G-T

36698196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29333786-T-C

36698388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29333969-G-T

http://identifiers.org/hco/6/GRCh38#36698715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29334307-C-A

36699001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334576-C-T

36699036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334589-C-T

36699261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334750-A-G

36699375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334813-C-G

36699436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334868-G-C

36699476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334903-T-C

36699568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29334979-C-T

36699610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29335021-C-T

36700887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29336146-G-A

36700887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29336146-G-C

36700952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29336207-G-T

36701028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29336277-T-C

36703632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29338392-C-T

http://identifiers.org/hco/6/GRCh38#36704131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29339706-C-A

36704131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29339706-C-T

36704177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29339767-G-T

36704198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29339790-G-A

36704198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29339790-G-T

36704338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29339930-C-T

http://identifiers.org/hco/6/GRCh38#36704384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29339976-C-A

36704384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29339976-C-T

http://identifiers.org/hco/6/GRCh38#36704450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29340042-C-A

36704450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29340042-C-T

http://identifiers.org/hco/6/GRCh38#36704573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29340157-C-A

36704573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29340157-C-T

36704619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29340203-T-C

36704673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29340257-C-G

36713710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350318-G-A

36713710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350318-G-T

36713775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350383-G-A

36713775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350383-G-T

36713796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350403-G-A

36713865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: stop gained
orthologous variants: 29350472-C-G

36713904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29350511-G-A

http://identifiers.org/hco/6/GRCh38#36713929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29350536-C-A

36713953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350560-T-C

36714232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29350750-C-T

36714865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29351280-C-T

36715165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29352382-G-T

36715366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29352567-G-T

36715619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29352752-A-G

36715619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29352752-A-T

36715840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29352893-G-A

36716022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29353013-C-T

36716116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29353092-A-G

36716540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29353173-C-T

36716632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29353263-C-G

36717125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29353774-T-C

36717246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354141-C-T

36717280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: stop gained
orthologous variants: 29354167-G-T

36717368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29354255-G-A

36717368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29354255-G-T

http://identifiers.org/hco/6/GRCh38#36717369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29354256-C-A

36717405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29354292-G-A

36717405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29354292-G-T

36717428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354315-G-A

36717428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354315-G-T

http://identifiers.org/hco/6/GRCh38#36717982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29354743-C-A

36717982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354743-C-T

http://identifiers.org/hco/6/GRCh38#36717990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29354751-C-A

36717990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354751-C-T

36717996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354757-G-A

http://identifiers.org/hco/6/GRCh38#36718029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29354790-C-A

36718029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 29354790-C-T

36718047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29354808-C-T

http://identifiers.org/hco/6/GRCh38#36718155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29354886-C-A

36718155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354886-C-G

36718155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354886-C-T

http://identifiers.org/hco/6/GRCh38#36718157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29354888-C-A

36718157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354888-C-G

36718157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354888-C-T

36718166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354905-T-C

36718196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354928-G-A

36718234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29354962-T-C

36718422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355174-T-C

36718434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355184-G-A

36718434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355184-G-T

http://identifiers.org/hco/6/GRCh38#36718461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29355211-C-A

36718461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355211-C-T

http://identifiers.org/hco/6/GRCh38#36718495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29355243-C-A

36718495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 29355243-C-G

36718495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 29355243-C-T

http://identifiers.org/hco/6/GRCh38#36718508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29355256-C-A

36718508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, missense_variant
orthologous variants: 29355256-C-G

36718508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29355256-C-T

36718601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355352-G-A

36718601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355352-G-T

36718609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29355360-G-C

36720215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29356814-G-A

36720215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29356814-G-C

36720215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29356814-G-T

http://identifiers.org/hco/6/GRCh38#36720226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29356825-A-C

36720226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29356825-A-T

http://identifiers.org/hco/6/GRCh38#36720232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29356833-A-C

36720232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29356833-A-T

36720330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29356920-G-T

36720429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: stop_gained, undefined
orthologous variants: 29357019-C-T

36720431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, undefined
orthologous variants: 29357021-G-T

36720434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous_variant, undefined
orthologous variants: 29357024-G-A

36720434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, undefined
orthologous variants: 29357024-G-T

36720449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29357039-G-A

36720449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29357039-G-T

36720452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29357042-T-C

36720533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29357129-G-A

36720533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29357129-G-T

36720606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357199-T-A

36720606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357199-T-G

36720621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357212-T-C

http://identifiers.org/hco/6/GRCh38#36720622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29357213-C-A

36720633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357224-T-A

36720633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357224-T-G

36720790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357797-T-C

36720883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357878-G-A

36720942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29357934-T-C

36721085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29358025-G-A

36721146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29358084-T-A

http://identifiers.org/hco/6/GRCh38#36721193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358131-C-A

36721270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358208-G-A

36721270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358208-G-T

http://identifiers.org/hco/6/GRCh38#36721291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358229-A-C

36721291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358229-A-G

http://identifiers.org/hco/6/GRCh38#36721319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358257-A-C

36721319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358257-A-G

http://identifiers.org/hco/6/GRCh38#36721328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358266-C-A

36721328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358266-C-T

http://identifiers.org/hco/6/GRCh38#36721380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358318-C-A

36721424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358362-G-A

36721424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358362-G-T

36721462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358403-A-G

36721497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358450-A-G

36721497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358450-A-T

36721560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358495-C-T

36721569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358504-C-T

36721879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358709-C-T

36721904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358734-G-A

36721904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358734-G-T

http://identifiers.org/hco/6/GRCh38#36721945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358760-C-A

36721945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358760-C-T

36722063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358878-G-A

http://identifiers.org/hco/6/GRCh38#36722074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358889-A-C

36722074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29358889-A-G

36722120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358935-G-A

36722120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358935-G-T

http://identifiers.org/hco/6/GRCh38#36722129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358944-C-A

36722129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29358944-C-T

http://identifiers.org/hco/6/GRCh38#36722156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29358971-C-A

36722257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359060-C-G

36722257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359060-C-T

http://identifiers.org/hco/6/GRCh38#36722295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29359086-C-A

36722295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359086-C-T

36722297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359088-A-G

36722297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359088-A-T

36722342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359133-T-C

36722360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359151-A-G

36722382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359173-G-A

36722382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359173-G-C

36722382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359173-G-T

36722495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359289-A-G

36722534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359328-G-C

36722534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29359328-G-T

36722573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359367-G-T

36722621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359412-C-T

36722642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: synonymous variant
orthologous variants: 29359433-C-T

36722744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29359535-T-A

36722744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29359535-T-G

36722771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29359556-G-C

36722771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29359556-G-T

http://identifiers.org/hco/6/GRCh38#36725702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29363322-C-A

36725702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363322-C-G

36725748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363367-A-G

36725748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363367-A-T

http://identifiers.org/hco/6/GRCh38#36725792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29363411-C-A

36725956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363556-G-A

http://identifiers.org/hco/6/GRCh38#36725997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29363598-C-A

36725997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363598-C-T

http://identifiers.org/hco/6/GRCh38#36726030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29363634-C-A

36726030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363634-C-G

36726030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363634-C-T

36726065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363669-A-G

36726065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363669-A-T

36726068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363672-G-A

36726068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363672-G-T

36726267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29363811-A-G

http://identifiers.org/hco/6/GRCh38#36727523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29364171-C-A

http://identifiers.org/hco/6/GRCh38#36727724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29364370-C-A

36727740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364386-G-A

36727740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364386-G-T

36727765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364415-T-A

36727765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364415-T-C

http://identifiers.org/hco/6/GRCh38#36727815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29364469-C-A

36727833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364488-G-A

36727833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364488-G-T

http://identifiers.org/hco/6/GRCh38#36728652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29364871-A-C

36728652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364871-A-T

36728689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29364903-T-G

36728825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365063-T-A

http://identifiers.org/hco/6/GRCh38#36728911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29365126-C-A

36728911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365126-C-G

36728967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365163-A-G

36729003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365202-G-A

36729003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365202-G-T

36729011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365210-A-G

36729033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365230-G-A

http://identifiers.org/hco/6/GRCh38#36729132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29365307-C-A

36729161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365335-A-G

36729501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29365680-G-T

36730613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29366288-G-A

36730613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29366288-G-T

36730624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29366299-T-C

http://identifiers.org/hco/6/GRCh38#36730705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29366354-C-A

36730705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 29366354-C-G

36730705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 29366354-C-T

36730729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 29366378-G-A

36730729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: missense variant
orthologous variants: 29366378-G-T

36730802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29366428-T-A

36730804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29366430-G-A

http://identifiers.org/hco/6/GRCh38#36730818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29366443-C-A

36731904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29367069-T-C

36731904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29367069-T-G

http://identifiers.org/hco/6/GRCh38#36731943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29367111-C-A

36731943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29367111-C-T

36731992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: intron variant
orthologous variants: 29367148-C-T

36732087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 29367243-C-T

36732103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: 29367259-C-T

http://identifiers.org/hco/6/GRCh38#36732108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29367264-C-A

http://identifiers.org/hco/6/GRCh38#36732136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29367292-C-A

36732136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: 29367292-C-T

http://identifiers.org/hco/6/GRCh38#36732188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29367331-C-A

36732188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: 29367331-C-T

36732189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21068
most severe consequence: 3 prime UTR variant
orthologous variants: 29367332-A-G